<?xml version="1.0"?>
<rss version="2.0">
   <channel>
      <title>Genetic Problems by </title>
      <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg</link>
      <description>In this Padlet, you will have the opportunity to walk through the steps of solving genetic problems.  All students are encouraged to use this tool to post their own genetic problems. Other students will be able to see and collaborate their own work and answers.  If your problem is complete and all of your group agrees on the answer, then you may post your final answer to the genetic assignment on Padlet.</description>
      <language>en-us</language>
      <pubDate>2018-07-11 16:07:17 UTC</pubDate>
      <lastBuildDate>2023-02-17 04:13:21 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url>https://padlet-assets.s3.amazonaws.com/icons/Bigthunderstorm.png</url>
      </image>
      <item>
         <title>1.       Notes </title>
         <author>jacordoba1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/269966544</link>
         <description><![CDATA[<div>1.  Rewrite the genetic problem<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2018-07-11 16:26:25 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/269966544</guid>
      </item>
      <item>
         <title>4.    Punnet Square</title>
         <author>jacordoba1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/269966863</link>
         <description><![CDATA[<div>4.  Fill out a Punnett Square to solve your problem<br><br></div><div>Ex; Mom and dad heterozygous for Curly hair  (If you can upload a pictur of your punnett square, do this, but if you can't describe, the cross.  You may describe the punnett by using the terms Quadrant 1 =BB, Quadrant 2= Bb (Reading from left to right, then proceeding to the next row)</div>]]></description>
         <enclosure url="http://upload.wikimedia.org/wikipedia/commons/thumb/1/17/Punnett_square_mendel_flowers.svg/550px-Punnett_square_mendel_flowers.svg.png" />
         <pubDate>2018-07-11 16:29:45 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/269966863</guid>
      </item>
      <item>
         <title>2.	Create a key </title>
         <author>jacordoba1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/270703189</link>
         <description><![CDATA[<div>2.  Dominant Allele and Recessive Allele. Include gender where gender is a factor in inheritance.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-07-20 12:43:21 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/270703189</guid>
      </item>
      <item>
         <title>3.     Writing down phenotypes and genotypes                                                         </title>
         <author>jacordoba1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/270703223</link>
         <description><![CDATA[<div> 3.   Write out phenotypes and genotypes of all the individuals involved                              <br>Ex; Mom Heterozygous for Curly hair; Aa         <br>Ex; Dad Heterozygous for Curly hair; Aa</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-07-20 12:44:20 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/270703223</guid>
      </item>
      <item>
         <title>5.      Interpret Results</title>
         <author>jacordoba1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/270703403</link>
         <description><![CDATA[<div>5.   Answer the question </div><div>Genotype;     AA : Aa : aa</div><div>Phenotype;    Curly :  Straight<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2018-07-20 12:47:58 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/270703403</guid>
      </item>
      <item>
         <title>Genetic Problem D</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/412996726</link>
         <description><![CDATA[<div>In humans, hair on the back of the hand is dominant over no hair. Bob, who has no hair, marries Sue, who has hair on the back of the hand. One of their three children, has hair on the back of the hand. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:13:59 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/412996726</guid>
      </item>
      <item>
         <title>Key for D</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/412997301</link>
         <description><![CDATA[<div><strong>D: </strong>Hair on back of hand<br><strong>d: </strong> No hair on back of hand</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:14:57 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/412997301</guid>
      </item>
      <item>
         <title>phenotype and genotype</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413003669</link>
         <description><![CDATA[<div><strong>Sue</strong> heterozygous for hair; <strong>Dd</strong><br><strong>Bob</strong> homozygous no hair; <strong>dd</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:23:03 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413003669</guid>
      </item>
      <item>
         <title>1.Genetic problem B:</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413004275</link>
         <description><![CDATA[<div>Sue, the mother has a recessive trait of no freckles, while Bob has a dominant trait for freckles. </div><div><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:24:05 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413004275</guid>
      </item>
      <item>
         <title>2. Key for B</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413004859</link>
         <description><![CDATA[<div> B: freckles on face             b: no freckles on face</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:24:57 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413004859</guid>
      </item>
      <item>
         <title>3.Phenotypes and Genotypes B</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413007423</link>
         <description><![CDATA[<div>Mom: Recessives Homozygous for freckles;bb <br><br>Dad: Dominant Heterozygous for freckles;Bb.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:29:22 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413007423</guid>
      </item>
      <item>
         <title>4.Punnet Square B</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413010384</link>
         <description><![CDATA[<div>In humans, freckles are dominant over no freckles. Bob, who Has freckles(B), marries Sue, who has no freckles(b). One of their three children has freckles. 3:1<br> </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/432806649/9f7e70675c5d0bf312008ff755751972/Freckles_2_5.png" />
         <pubDate>2019-11-18 20:34:39 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413010384</guid>
      </item>
      <item>
         <title>punnett square</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413010779</link>
         <description><![CDATA[<div> Sue: Heterozygous for hair<br>Bob: Homozygous recessive for no hair<br><strong>Key</strong></div><div>D- Hair on back of hand<br>d- No hair on back of hand</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/432810832/4fb70ffe14a6ef6c771e8a3bdfa0eb6d/bm2l4bimage16.jpg" />
         <pubDate>2019-11-18 20:35:26 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413010779</guid>
      </item>
      <item>
         <title>Key for H</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413017633</link>
         <description><![CDATA[<div>H: functioning gene<br>h: mutation</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:47:50 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413017633</guid>
      </item>
      <item>
         <title>Phenotypes and Geneotypes for H</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413018356</link>
         <description><![CDATA[<div>Dad:  Homozygous for Cystic Fibrosis: hh<br><br>Mom: Heterozygous for Cystic Fibrosis:  Hh</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:49:17 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413018356</guid>
      </item>
      <item>
         <title>5. Interpret Results B</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413021757</link>
         <description><![CDATA[<div>Genotype: Bb, bb<br><br>Phenotype: Freckles, No Freckles</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 20:56:04 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413021757</guid>
      </item>
      <item>
         <title></title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413027930</link>
         <description><![CDATA[Cystic fibrosis is a sex linked disorder. Bob, who has Cystic fibrosis, marries Sue, who does not have Cystic fibrosis.  What is the chances of a child of theirs having the disorder and the chances of any child carrying the disorder? ]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:06:51 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413027930</guid>
      </item>
      <item>
         <title>Genetic problem E</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413028393</link>
         <description><![CDATA[<div>Cystic fibrosis is a sex linked disorder. Bob, who has Cystic fibrosis, marries Sue, who does not have Cystic fibrosis.  What is the chances of a child of theirs having the disorder and the chances of any child carrying the disorder? </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:07:27 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413028393</guid>
      </item>
      <item>
         <title>Genetic Problem  H</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413030327</link>
         <description><![CDATA[<div>Cystic fibrosis is a sex linked disorder. Bob, who has Cystic fibrosis, marries Sue, who is a carrier for Cystic fibrosis.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:11:14 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413030327</guid>
      </item>
      <item>
         <title>Genetic Problem E </title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413033112</link>
         <description><![CDATA[<div>Create Key<br>Dominant Allele Sue- "E" <br>Recessive Allele Bob- "e"<br>E- normal<br>e- cystic fibrosis </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:16:57 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413033112</guid>
      </item>
      <item>
         <title>Punnett Square H</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413035314</link>
         <description><![CDATA[<div>Bob Is Homozygous recessive Cystic Fibrosis (cc)<br><br>Mom is Heterozygous for normal gene (Cc)</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/432822408/828c5022d70d00e40aa904ba61780cfb/genotype_H.jpg" />
         <pubDate>2019-11-18 21:21:30 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413035314</guid>
      </item>
      <item>
         <title>Interpret Results H</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413037012</link>
         <description><![CDATA[<div>Genotype: two heterozygous children and two Homozygous recessive<br><br>Phenotype: 50% Normal children 50% Children with Cystic Fibrosis </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:24:34 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413037012</guid>
      </item>
      <item>
         <title>Genetic problem C</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413037353</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:25:16 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413037353</guid>
      </item>
      <item>
         <title>Genetic Problem E </title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413037646</link>
         <description><![CDATA[<div>Genotypic &amp; Phenotypic<br> Mom is homozygous dominant for cystic fibrosis. "EE"<br>Dad is homozygous recessive. "ee"</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:25:39 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413037646</guid>
      </item>
      <item>
         <title>interpret results D</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413041344</link>
         <description><![CDATA[<div>Genotype: two heterozygous children, and two homozygous recesive<br>phenotype; 50 % with hair, and 50% without hair</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:32:20 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413041344</guid>
      </item>
      <item>
         <title>Genetic Problem E</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413044604</link>
         <description><![CDATA[<div>Punnet Square</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/432817223/e17d849d7779c8f8acd277380c44263a/Cystic_Fibrosis.png" />
         <pubDate>2019-11-18 21:39:04 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413044604</guid>
      </item>
      <item>
         <title>Genetic Problem E </title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413046802</link>
         <description><![CDATA[<div>Genotype- 100%<br>Phenotype- All would be normal </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-18 21:43:28 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413046802</guid>
      </item>
      <item>
         <title>Genetic F Problem</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413635630</link>
         <description><![CDATA[<div>Bob is color blind and is married to sue who isn't color blind but we do not know if she's a carrier. what is the genetypic and phenotypic of sue (FF/Ff) and bob's (ff) kids who will carry the disorder? </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-19 20:01:29 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413635630</guid>
      </item>
      <item>
         <title>Key Genetic problem F</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413649317</link>
         <description><![CDATA[<div>F -- not color blind<br>f -- color blind</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-19 20:23:09 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413649317</guid>
      </item>
      <item>
         <title>Genetic Problem F </title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413650841</link>
         <description><![CDATA[<div>Bob homozygous for colorblindness ff<br>Sue homozygous or heterozygous FF / Ff</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-19 20:25:38 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413650841</guid>
      </item>
      <item>
         <title>Punnet Square genetic problem F</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413653671</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/433288438/9048230db45dc5d7060adda52f3526c0/drawing.png" />
         <pubDate>2019-11-19 20:30:04 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413653671</guid>
      </item>
      <item>
         <title>genetic problem F</title>
         <author></author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413658968</link>
         <description><![CDATA[<div>Genotype; Ff:ff<br>Phenotype; not colorblind : colorblind</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-19 20:38:53 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413658968</guid>
      </item>
      <item>
         <title>Genetic Problem A</title>
         <author>EllieAleman</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413805707</link>
         <description><![CDATA[<div>In people, having a cleft chin is a dominant gene and smooth chins are recessive. Bob has a cleft chin, his wife Sue has a smooth chin. Out of their three children one has a smooth chin. Using the Punnet Square it shows the cross between each phenotype and gives the genotype and phenotype ratios.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 04:06:12 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413805707</guid>
      </item>
      <item>
         <title></title>
         <author>EllieAleman</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413807181</link>
         <description><![CDATA[<div>Bob- Heterozygous dominant for cleft chin; Aa<br>Sue- Homozygous recessive for smooth chin </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 04:13:38 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413807181</guid>
      </item>
      <item>
         <title>GENETIC PROBLEM D</title>
         <author>rmartinez_4049</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413808223</link>
         <description><![CDATA[<div>In humans, hair on the back of the hand is dominant over no hair. Bob, who has no hair, marries Sue, who has hair on the back of the hand. One of their three children, has hair on the back of the hand. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 04:19:09 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413808223</guid>
      </item>
      <item>
         <title>KEY genetic problem D</title>
         <author>rmartinez_4049</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413809704</link>
         <description><![CDATA[<div>D - hair on back of hand<br>d - no hair on back of hand</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 04:27:41 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413809704</guid>
      </item>
      <item>
         <title>GENOTYPES AND PHENOTYPES genetic problem D</title>
         <author>rmartinez_4049</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413810089</link>
         <description><![CDATA[<div>Sue  heterozygous for hair on the back of the hand; Dd<br>Bob  homozygous for no hair on the back of the hand; dd</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 04:29:59 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413810089</guid>
      </item>
      <item>
         <title>PUNNET SQUARE genetic problem D</title>
         <author>rmartinez_4049</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413812121</link>
         <description><![CDATA[<div>KEY<br>D hair on back of hand<br>d no hair on back of hand</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/432138839/6191af4caf059554269cc502a704ac72/punnet_square.jpg" />
         <pubDate>2019-11-20 04:42:42 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413812121</guid>
      </item>
      <item>
         <title>RESULTS genetic problem D</title>
         <author>rmartinez_4049</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413812559</link>
         <description><![CDATA[<div>Genotype; Dd:dd<br>                      1:1<br>Phenotype; hair on back of hand: no hair on back of hand<br><br>Probability that 50% of children will have hair on the back of the hand while 50% will not have hair on the back of the hand.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 04:45:12 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/413812559</guid>
      </item>
      <item>
         <title>Punnet Square  </title>
         <author>jose_alva2502</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414311799</link>
         <description><![CDATA[<div><br><br></div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/433766184/f6417307e95f0599632f24c9a3d2ea87/drawing.png" />
         <pubDate>2019-11-20 20:49:07 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414311799</guid>
      </item>
      <item>
         <title>KEY</title>
         <author>NestorAlt</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414321248</link>
         <description><![CDATA[<div>A-Cleft Chin<br>a-Smooth Chin</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 21:05:53 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414321248</guid>
      </item>
      <item>
         <title>KEY</title>
         <author>NestorAlt</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414322049</link>
         <description><![CDATA[<div>A- Cleft Chin<br>a- Smooth Chin</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 21:07:27 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414322049</guid>
      </item>
      <item>
         <title></title>
         <author>jose_alva2502</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414324281</link>
         <description><![CDATA[<div>Genotype 2 : 2 ratio<br>Phenotype 2 : 2 ratio</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-20 21:12:00 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414324281</guid>
      </item>
      <item>
         <title>Genetic Problem B</title>
         <author>abigailmtz303</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414860723</link>
         <description><![CDATA[<div>Ocular albinism is a recessive gene which causes a person to lack melanin pigment in the persons eyes only. Bob who is affected by ocular albinism is married to Sue who is a carrier for ocular albinism. What is will be the ratio of ocular albinism to normal children if Sue and Bob were to have kids.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 18:31:06 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414860723</guid>
      </item>
      <item>
         <title>Key Genetic Problem B</title>
         <author>abigailmtz303</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414867609</link>
         <description><![CDATA[<div>B - no ocular albinism<br>b - ocular albinism<br>the mutation for ocular albinism occurs on the X-chromosome making men more susceptible to being affected by the mutation.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 18:39:39 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414867609</guid>
      </item>
      <item>
         <title>Genotypes and Phenotypes B</title>
         <author>abigailmtz303</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414879679</link>
         <description><![CDATA[<div>Bob has ocular albinism which affects his singular X-chromosome; b<br>Sue is heterozygous for ocular albinism; Bb</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 18:53:41 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414879679</guid>
      </item>
      <item>
         <title>Punnett Square</title>
         <author>abigailmtz303</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414882150</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/434168496/437466f5a44944a1ecfe3adf4254b71f/drawing.png" />
         <pubDate>2019-11-21 18:58:11 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414882150</guid>
      </item>
      <item>
         <title>Interpret Results</title>
         <author>abigailmtz303</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414886977</link>
         <description><![CDATA[<div>Genotype; Bb : B : bb : b<br>                        1:1:1:1<br>Phenotype; no ocular albinism: ocular albinism<br><br>There is a 50% chance for the kids to be affected by ocular albinism for both male and female children.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 19:03:22 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414886977</guid>
      </item>
      <item>
         <title>1. Genetic Assignment I</title>
         <author>crivera1613</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414943437</link>
         <description><![CDATA[<div>Suppose that Donna is colorblind but Darrel is not. If Donna and Darrel have a family, what percentage of their boys will be colorblind?</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 20:19:58 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414943437</guid>
      </item>
      <item>
         <title>2. Key for I</title>
         <author>crivera1613</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414945507</link>
         <description><![CDATA[<div>K - Not colorblind<br>k - Colorblind</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 20:23:32 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414945507</guid>
      </item>
      <item>
         <title>3. Phenotypes and Genotypes for I</title>
         <author>crivera1613</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414947093</link>
         <description><![CDATA[<div>Darrel homozygous dominant: KK: Not colorblind<br>Donna homozygous recessive: kk: Colorblind</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 20:26:30 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414947093</guid>
      </item>
      <item>
         <title>Punnett Square</title>
         <author>brando_barberena</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414957437</link>
         <description><![CDATA[<div>P</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/434222783/8b5b275b31c5f485fbfbc226e5fa9059/IMG_1803_1_.jpg" />
         <pubDate>2019-11-21 20:45:48 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414957437</guid>
      </item>
      <item>
         <title>Interpret Results</title>
         <author>brando_barberena</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414968475</link>
         <description><![CDATA[<div><br>Genotype: 100% Heterozygous<br>Phenotype: 100% Colored Vision</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-21 21:08:05 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/414968475</guid>
      </item>
      <item>
         <title>Genetic Problem F</title>
         <author>marialopez_1201</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415301477</link>
         <description><![CDATA[<div>Color Blind is a sex linked disorder. Bob, who is color blind, marries Sue, who is not color blind .What is the chances of a child of theirs having the disorder and the chances of any child carrying the disorder. Using the Punnett square, show the cross, and give the genotypic and phenotypic ratios for the other children.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-22 15:10:51 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415301477</guid>
      </item>
      <item>
         <title>Key Genetic Problem F</title>
         <author>marialopez_1201</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415302866</link>
         <description><![CDATA[<div>F- Not color blind<br>f- Color blind</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-22 15:12:49 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415302866</guid>
      </item>
      <item>
         <title>Sue heterozygous for not color blind; Ff</title>
         <author>marialopez_1201</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415307629</link>
         <description><![CDATA[<div>Bob homozygous for color blind; ff</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-22 15:19:41 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415307629</guid>
      </item>
      <item>
         <title>Punnet Square</title>
         <author>marialopez_1201</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415309933</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/434477269/b4d456e701b3d0a0434835b1e9c5923a/drawing.png" />
         <pubDate>2019-11-22 15:22:49 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415309933</guid>
      </item>
      <item>
         <title></title>
         <author>marialopez_1201</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415310646</link>
         <description><![CDATA[<div>Genotype; Ff 2:2 ratio<br>Phentotype; ff 2:2 ratio</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-22 15:23:49 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/415310646</guid>
      </item>
      <item>
         <title>genetic assignment B </title>
         <author>aalyahcotter1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416489066</link>
         <description><![CDATA[<div>In humans, freckles are dominant over no freckles. Bob, who </div><div>Has freckles, marries Sue, who has no freckles. One of their  three children has freckles.                   </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 03:28:12 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416489066</guid>
      </item>
      <item>
         <title>The Key </title>
         <author>aalyahcotter1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416489464</link>
         <description><![CDATA[<div>B - Freckles <br>b- no freckles </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 03:30:42 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416489464</guid>
      </item>
      <item>
         <title>Genotypes and Phenotypes </title>
         <author>aalyahcotter1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416490169</link>
         <description><![CDATA[<div>Sue mom is homozygous for no freckles; bb<br>Bob the dad is heterozygous for freckles; Bb  </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 03:35:14 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416490169</guid>
      </item>
      <item>
         <title>Punnett square </title>
         <author>aalyahcotter1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416491039</link>
         <description><![CDATA[<div>   </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/435486060/cda2ed7016c225835a0b14d2e230de38/Screen_Shot_2019_11_25_at_9_49_04_PM.png" />
         <pubDate>2019-11-26 03:40:09 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416491039</guid>
      </item>
      <item>
         <title>Results </title>
         <author>aalyahcotter1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416492959</link>
         <description><![CDATA[<div>Genotype Bb:bb, 2:2 <br><br>There was a 50% chance that either of the 3 Childs would come out with or without freckles in this case the both homozygous recessive gene were in two children with no freckles and the only child with freckles has the heterozygous gene for freckles. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 03:50:01 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416492959</guid>
      </item>
      <item>
         <title>Genetic Assignment C:</title>
         <author>fguerr42</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416690111</link>
         <description><![CDATA[<div>In humans, unattached ears are dominant over attached. Bob marries Sue, but Bob has attached ears while Sue has unattached. One of their offspring ended up with attached ears. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 14:38:37 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416690111</guid>
      </item>
      <item>
         <title>The Key:</title>
         <author>fguerr42</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416690876</link>
         <description><![CDATA[<div>E- Unattached Ears<br>e- Attached Ears</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 14:39:48 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416690876</guid>
      </item>
      <item>
         <title>Genotypes and Phenotypes:</title>
         <author>fguerr42</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416691418</link>
         <description><![CDATA[<div>Mom, Sue, is heterozygous for unattached ears, while Dad, Bob, is homozygous for attached ears </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 14:40:44 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416691418</guid>
      </item>
      <item>
         <title>Punnet Square:</title>
         <author>fguerr42</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416693574</link>
         <description><![CDATA[<div>         E      e<br>e   [ Ee ][ ee ]<br>e   [ Ee ][ ee ]</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 14:43:48 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416693574</guid>
      </item>
      <item>
         <title>Results:</title>
         <author>fguerr42</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416699523</link>
         <description><![CDATA[<div>Genotype Ee:ee, 2:2<br>Phenotype: 2/4 Unattached ears and 2/4 Attached ears.<br>According to the punnet square, there was a 50% chance out of four offspring would come out with unattached or attached ears. The only child, so far out of the three, carries a recessive gene. There is another chance their fourth child will display the recessive gene for attached ears. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-26 14:52:23 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416699523</guid>
      </item>
      <item>
         <title>Genetic Problem E </title>
         <author>jhern778</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416969684</link>
         <description><![CDATA[<div>Cystic fibrosis is a sex linked disorder. Bob, who has Cystic fibrosis, marries Sue, who does not have Cystic fibrosis.  If they were to have a child, what would be the chances of a child having the disorder and the chances of any child carrying the trait?</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 02:21:00 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416969684</guid>
      </item>
      <item>
         <title>Genetic Problem E</title>
         <author>jhern778</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416970659</link>
         <description><![CDATA[<div>Key<br>Dominant Allele: E (Sue)<br>Recessive Allele: e (Bob) <br>E: No Cystic Fibrosis<br>e: Cystic Fibrosis</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 02:26:08 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416970659</guid>
      </item>
      <item>
         <title>Genetic Problem E</title>
         <author>jhern778</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416971153</link>
         <description><![CDATA[<div>Genotype and Phenotype<br>Sue is homozygous dominant for EE: No cystic fibrosis<br>Bob is homozygous recessive for ee: Cystic Fibrosis<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 02:28:51 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416971153</guid>
      </item>
      <item>
         <title>Genetic Problem E</title>
         <author>jhern778</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416972674</link>
         <description><![CDATA[<div>Punnet Square</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/432237102/445eea3ec863f7b756d4beec8b9575bf/punnet_Square.png" />
         <pubDate>2019-11-27 02:36:00 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416972674</guid>
      </item>
      <item>
         <title>Genetic Problem E</title>
         <author>jhern778</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416976185</link>
         <description><![CDATA[<div>Interpret Results<br>Phenotype : 100% No Cystic Fibrosis<br>Genotype : Every offspring would have Ee </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 02:51:50 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416976185</guid>
      </item>
      <item>
         <title>Punnet Square G</title>
         <author>anapatricia_angulo</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416979443</link>
         <description><![CDATA[<div>             G          g                        g   {Gg}  {gg}<br>      g    {Gg}   {gg}</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 03:06:18 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416979443</guid>
      </item>
      <item>
         <title>Rewrite G</title>
         <author>anapatricia_angulo</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416986961</link>
         <description><![CDATA[<div>Color Blind is a sex linked disorder. Bob, who is color blind, marries Sue, who is a carrier for color blindness. What are the chances of a child of theirs having disorder and the chances of any child carrying the disorder? </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 03:40:51 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416986961</guid>
      </item>
      <item>
         <title>Key G</title>
         <author>anapatricia_angulo</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416987827</link>
         <description><![CDATA[<div>G- Color Blind<br>g- Not Color Blind</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 03:45:46 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416987827</guid>
      </item>
      <item>
         <title>Genotypes &amp; Phenotypes G  </title>
         <author>anapatricia_angulo</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416989095</link>
         <description><![CDATA[<div>Mom is Heterozygous for Color Bindness, Gg, and Dad is Homozygous, gg, for not Color Blindness. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 03:52:15 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416989095</guid>
      </item>
      <item>
         <title>Results G</title>
         <author>anapatricia_angulo</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416990077</link>
         <description><![CDATA[<div>Genotype- 2:2 ratio<br>Phenotype- 2:2 ratio<br>There is a 50% chance the children will be Color Blind, and there is a 50% chance that the children will not be Color Blind. </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-11-27 03:57:33 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/416990077</guid>
      </item>
      <item>
         <title>Group H: Cystic Fibrosis Genetic problem. </title>
         <author>dzamarri1</author>
         <link>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/421106968</link>
         <description><![CDATA[<div>Cystic fibrosis is a sex linked disorder. Bob, who has Cystic fibrosis, marries Sue, who is a carrier for Cystic fibrosis.  What are the chances of a child of theirs having the disorder and the chances of any child carrying the disorder?  Using the Punnett square, show the cross, and give the genotypic and phenotypic ratios for the other children.              KEY</div><div>H – Normal</div><div>h– Cystic fibrosis </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/437698712/7b35e68b7f91a9bec302b162de502190/Group_H_pic_1_of_punnett.png" />
         <pubDate>2019-12-07 01:34:43 UTC</pubDate>
         <guid>https://padlet.com/jacordoba1/rb6ji6bnv5zg/wish/421106968</guid>
      </item>
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