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Y-microdeletions: a review of the genetic basis for this common cause of male infertility
The human Y-chromosome contains genetic material responsible for normal testis development and spermatogenesis. The long arm (Yq) of the Y-chromosome has been found to be susceptible to self-recombination during spermatogenesis predisposing this area to deletions. The incidence of these deletions is...
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| Vydáno v: | Transl Androl Urol |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
AME Publishing Company
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8039600/ https://ncbi.nlm.nih.gov/pubmed/33850774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/tau-19-599 |
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