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      <title>Sugukromosoomide häired by Helen Semilarski</title>
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      <description>Rühmatöö</description>
      <language>en-us</language>
      <pubDate>2017-10-04 09:38:06 UTC</pubDate>
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         <title>XXY</title>
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         <link>https://padlet.com/helen_semilarski/12b/wish/193777873</link>
         <description><![CDATA[<div>Klinefelteri=XXY-sündroom</div>]]></description>
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         <pubDate>2017-10-04 10:22:34 UTC</pubDate>
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         <title>XXY-sündroom</title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193777878</link>
         <description><![CDATA[<div>Sümptom: vähene testosteroon, esineb meestel 1:500-1000</div>]]></description>
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         <pubDate>2017-10-04 10:22:36 UTC</pubDate>
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         <title>Turneri sündroom </title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193778001</link>
         <description><![CDATA[<div>Naisel vaid üks X kromosoom. </div>]]></description>
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         <pubDate>2017-10-04 10:23:04 UTC</pubDate>
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         <title>XYY-sündeoom </title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193778308</link>
         <description><![CDATA[<div>esineb ühel mehel&nbsp; 700-1000 kohta, võib esineda veidi väiksem intellekt ja käitumishäired</div>]]></description>
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         <pubDate>2017-10-04 10:24:12 UTC</pubDate>
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         <title>XXX</title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193778438</link>
         <description><![CDATA[<div>Naisel 3 xxx kromosoomi</div>]]></description>
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         <pubDate>2017-10-04 10:24:40 UTC</pubDate>
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         <title>Sportlased</title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193778555</link>
         <description><![CDATA[<div>Mõnikord on tekkinud kahtlusi võistlejate soo suhtes. Sooküsimuse keerulisust näitab see, et kontrolluuringutesse kaasati günekolooge, endokrinolooge, spordiarste ja psühholooge</div>]]></description>
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         <pubDate>2017-10-04 10:25:03 UTC</pubDate>
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         <title>X-liitelised dominantsed tunnused</title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193778761</link>
         <description><![CDATA[<div>Fragiilne Xi sündroom, mis tähendab päriliku vaimse arengu mahajäämist ning autismi</div>]]></description>
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         <pubDate>2017-10-04 10:25:49 UTC</pubDate>
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         <title>XX mehed (Chapelle&#39;i sündroom) ja XY naised (Swyeri sündroom)</title>
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         <pubDate>2017-10-04 10:27:06 UTC</pubDate>
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         <title></title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193779541</link>
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         <pubDate>2017-10-04 10:28:45 UTC</pubDate>
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         <title></title>
         <author></author>
         <link>https://padlet.com/helen_semilarski/12b/wish/193780541</link>
         <description><![CDATA[<div>Varem arvati ekslikult, et XYY-kromosoomide komplekt muudab mehed vägivaldseks ja annab neile kuritegevuslikud kalduvused ning lootele vastava diagnoosi saanud emadele soovitati aborti. Uuemad uurimused on näidanud, et need eelarvamused olid valed ja enamikul XYY-mee</div>]]></description>
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         <pubDate>2017-10-04 10:32:39 UTC</pubDate>
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