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  <author_name>ryamada22</author_name>
  <author_url>https://blog.hatena.ne.jp/ryamada22/</author_url>
  <blog_title>ryamadaの遺伝学・遺伝統計学メモ</blog_title>
  <blog_url>https://ryamada22.hatenablog.jp/</blog_url>
  <categories>
    <anon>論文</anon>
    <anon>疾患関連遺伝子解析</anon>
    <anon>関連解析</anon>
    <anon>文献</anon>
    <anon>ぱらぱらめくるシリーズ</anon>
    <anon>性差</anon>
  </categories>
  <description>[http://www.nature.com/nrg/journal/v9/n12/abs/nrg2415.html:title=Sex-specific genetic architecture of human disease. C Ober et al. nat reviews genet 9:911-922 2008] 遺伝的性差（ＸＸ保有対ＸＹ保有）と、形質発現との関係を調べることは２本立て。 性染色体→個体の性的差異(構造・内分泌・免疫、他)→疾患の性差 性染色体→疾患の性差 eQTLの利用も有効か。</description>
  <height>190</height>
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  <image_url></image_url>
  <provider_name>Hatena Blog</provider_name>
  <provider_url>https://hatena.blog</provider_url>
  <published>2009-03-28 14:20:25</published>
  <title>性差 sexual dimorphism</title>
  <type>rich</type>
  <url>https://ryamada22.hatenablog.jp/entry/20090328/1238304025</url>
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