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Matches in SemOpenAlex for { <https://semopenalex.org/work/W2123201599> ?p ?o ?g. }

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• W2123201599 abstract "BACKGROUNDCongenital bilateral absence of the vas deferens (CBAVD) is a distinct clinical entity accounting for ∼25% of obstructive azoospermia in infertile men. The association between CBAVD and mutated CFTR (cystic fibrosis transmembrane conductance regulator) alleles is well demonstrated in Caucasians, but the identity of CBAVD-susceptibility genes remains elusive in Asians. We investigate genomic copy number variations (CNVs) in a patient cohort of Taiwan." @default.
• W2123201599 created "2016-06-24" @default.
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• W2123201599 date "2008-12-04" @default.
• W2123201599 modified "2023-10-17" @default.
• W2123201599 title "Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens" @default.
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• W2123201599 doi "https://doi.org/10.1093/humrep/den413" @default.
• W2123201599 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19095672" @default.
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