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Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population.

<h4>Background</h4>Genetic causes of male infertility are hypothesized to involve multiple types of mutations, from single gene defects to complex chromosome rearrangements. Recently, several recurrent X-chromosome microdeletions (located in subtelomeric region of the long arm) were reported to be a...

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Detaylı Bibliyografya
Asıl Yazarlar: Blanka Chylíková, Ivan Hrdlička, Kamila Veselá, Karel Řežábek, František Liška
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science (PLoS) 2016-01-01
Seri Bilgileri:PLoS ONE
Online Erişim:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0156102&type=printable
Etiketler: Etiketle
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