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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...
Tallennettuna:
| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer US
2013
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| Aiheet: | |
| Linkit: | 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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