Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
about
Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humansSpermCheck Fertility, an immunodiagnostic home test that detects normozoospermia and severe oligozoospermiac.822+126T>G/C: a novel triallelic polymorphism of the TSSK6 gene associated with spermatogenic impairment in a Chinese population.Meiotic recombination and male infertility: from basic science to clinical reality?
P2860
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
@en
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
@nl
type
label
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
@en
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
@nl
prefLabel
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
@en
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.
@nl
P2093
P2860
P1476
Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment
@en
P2093
P2860
P356
10.1080/19396360701883266
P50
P577
2008-03-01T00:00:00Z