Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

Background: Complete deletion of the complete AZFc interval of the Y chromosome is the most common known genetic cause of human male infertility. Two partial AZFc deletions (gr/gr and b1/b3) that remove some copies of all AZFc genes have recently been identified in infertile and fertile populations,...

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מידע ביבליוגרפי
Main Authors: Machev, N, Saut, N, Longepied, G, Terriou, P, Navarro, A, Levy, N, Guichaoua, M, Metzler-Guillemai..., C, Collignon, P, Frances, A, Belougne, J, Clemente, E, Chiaroni, J, Chevillard, C, Durand, C, Ducourneau, A, Pech, N, McElreavey, K, Mattei, M, Mitchell, M
פורמט: Artigo
שפה:Inglês
יצא לאור: BMJ Group 2004
נושאים:
Original Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735624/
https://ncbi.nlm.nih.gov/pubmed/15520406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.022111
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