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2012 | 1 |
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Spermatogenic failure and the Y chromosome.
Hum Genet. 2017 May;136(5):637-655. doi: 10.1007/s00439-017-1793-8. Epub 2017 Apr 29.
Hum Genet. 2017.
PMID: 28456834
Review.
Its highly repetitive structure predisposes this chromosome to deletion/duplication events and is responsible for Y-linked copy-number variations (CNVs) with clinical relevance. The AZF deletions remove genes with predicted spermatogenic function en block and are the most …
Its highly repetitive structure predisposes this chromosome to deletion/duplication events and is responsible for Y-linked copy-number varia …
Autosomal mutations and human spermatogenic failure.
El Inati E, Muller J, Viville S.
El Inati E, et al.
Biochim Biophys Acta. 2012 Dec;1822(12):1873-9. doi: 10.1016/j.bbadis.2012.07.006. Epub 2012 Jul 27.
Biochim Biophys Acta. 2012.
PMID: 22841926
Free article.
Review.
Despite 3 years of assisted reproductive activities, a considerable number of cases (25-30%) remain idiopathic. This situation can be explained by a poor understanding of the basic mechanisms driving male and female gametogenesis. ...This article is part of a Special Issue …
Despite 3 years of assisted reproductive activities, a considerable number of cases (25-30%) remain idiopathic. This situation can be …
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Prognostic value of Y deletion analysis: what is the clinical prognostic value of Y chromosome microdeletion analysis?
Krausz C, Quintana-Murci L, McElreavey K.
Krausz C, et al.
Hum Reprod. 2000 Jul;15(7):1431-4. doi: 10.1093/humrep/15.7.1431.
Hum Reprod. 2000.
PMID: 10875846
Review.
Y microdeletion screening is therefore important, not only to define the aetiology of spermatogenic failure, but also because it gives precious information for a more appropriate clinical management of both the infertile male and his future male child....
Y microdeletion screening is therefore important, not only to define the aetiology of spermatogenic failure, but also because …
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