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Quoted phrase not found in phrase index: "Spermatogenic failure, X-linked, 3"
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Genomic testing for copy number and single nucleotide variants in spermatogenic failure.
Hardy J, Pollock N, Gingrich T, Sweet P, Ramesh A, Kuong J, Basar A, Jiang H, Hwang K, Vukina J, Jaffe T, Olszewska M, Kurpisz M, Yatsenko AN. Hardy J, et al. J Assist Reprod Genet. 2022 Sep;39(9):2103-2114. doi: 10.1007/s10815-022-02538-5. Epub 2022 Jul 18. J Assist Reprod Genet. 2022. PMID: 35849255 Free PMC article.
PURPOSE: To identify clinically significant genomic copy number (CNV) and single nucleotide variants (SNV) in males with unexplained spermatogenic failure (SPGF). MATERIALS AND METHODS: Peripheral blood DNA from 97/102 study participants diagnosed with oligozoosperm …
PURPOSE: To identify clinically significant genomic copy number (CNV) and single nucleotide variants (SNV) in males with unexplained sper …
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 …