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Y chromosome microdeletions in infertile men: prevalence, phenotypes and screening markers for the Indian population

PURPOSE: Yq microdeletions are the leading genetic cause of male infertility and its detection is clinically relevant for appropriate genetic counseling. We aimed to determine the prevalence and type of Yq microdeletions, the associated seminal phenotypes and the STS markers that are relevant for it...

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Detaylı Bibliyografya
Asıl Yazarlar: Sen, S., Pasi, A. R., Dada, R., Shamsi, M. B., Modi, D.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer US 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3607676/
https://ncbi.nlm.nih.gov/pubmed/23344732
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-013-9933-0
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