Yüklüyor......

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

BACKGROUND: 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 associat...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Chylíková, Blanka, Hrdlička, Ivan, Veselá, Kamila, Řežábek, Karel, Liška, František
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4892532/
https://ncbi.nlm.nih.gov/pubmed/27257673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0156102
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!