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      <title>Hemophilia by Gerardo Pacheco Loya</title>
      <link>https://padlet.com/s80331/vy7btjs89qup</link>
      <description>Genetic disorder
</description>
      <language>en-us</language>
      <pubDate>2019-03-12 20:56:41 UTC</pubDate>
      <lastBuildDate>2025-12-12 15:14:29 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>frequency</title>
         <author>s80331</author>
         <link>https://padlet.com/s80331/vy7btjs89qup/wish/340639256</link>
         <description><![CDATA[<div>The two major forms of hemophilia occur much more commonly in males than in females. Hemophilia A is the most common type of the condition; 1 in 4,000 to 1 in 5,000 males worldwide are born with this disorder. Hemophilia B occurs in approximately 1 in 20,000 newborn males worldwide.</div>]]></description>
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         <pubDate>2019-03-12 21:23:54 UTC</pubDate>
         <guid>https://padlet.com/s80331/vy7btjs89qup/wish/340639256</guid>
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         <title>inheritance pattern</title>
         <author>s80331</author>
         <link>https://padlet.com/s80331/vy7btjs89qup/wish/340639937</link>
         <description><![CDATA[<div>Hemophilia A and hemophilia B are inherited in an <a href="https://ghr.nlm.nih.gov/art/large/xlinkrecessive.jpeg">X-linked recessive pattern</a>. The genes associated with these conditions are located on the <a href="https://ghr.nlm.nih.gov/chromosome/X">X chromosome</a>, which is one of the two <a href="https://ghr.nlm.nih.gov/art/large/sex-chromosomes-x-and-y.jpeg">sexchromosomes</a></div>]]></description>
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         <pubDate>2019-03-12 21:27:09 UTC</pubDate>
         <guid>https://padlet.com/s80331/vy7btjs89qup/wish/340639937</guid>
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