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Quoted phrase not found in phrase index: "Spermatogenic failure, X-linked, 3"
Page 1
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.
PLoS Genet. 2013 Mar;9(3):e1003349. doi: 10.1371/journal.pgen.1003349. Epub 2013 Mar 21.
PLoS Genet. 2013.
PMID: 23555275
Free PMC article.
After assaying genomewide SNPs and CNVs in 323 Caucasian men with idiopathic spermatogenic impairment and more than 1,100 controls, we estimate that each rare autosomal deletion detected in our study multiplicatively changes a man's risk of disease by 10% (OR 1.10 [1.04-1. …
After assaying genomewide SNPs and CNVs in 323 Caucasian men with idiopathic spermatogenic impairment and more than 1,100 controls, w …
Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure.
Shen Y, Xu J, Yang X, Liu Y, Ma Y, Yang D, Dong Q, Yang Y.
Shen Y, et al.
Biol Reprod. 2017 Mar 1;96(3):610-616. doi: 10.1093/biolre/iox006.
Biol Reprod. 2017.
PMID: 28339631
Spermatogenic failure characterized by impaired sperm production is a common multifactorial disease with molecular and cytogenetic causes for its extreme phenotype that include azoospermia and severe oliogzoospermia. ...To confirm their spermatogenic effect, …
Spermatogenic failure characterized by impaired sperm production is a common multifactorial disease with molecular and cytogen …
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