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Molecular Study of（TG）m（T）n Polymorphisms in Iranian Males With Congenital Bilateral Absence of the Vas Deferens
CBAVD CFTR IVS8-5T male infertility
2008/12/24
Congenital bilateral absence of the vas deferens (CBAVD) is a frequent cause of obstructive azoospermia. Nearly 75% of men with CBAVD have at least 1 detectable common mutation in the cystic fibr...
Identification of Polymorphisms in the Hrb, GOPC, and Csnk2a2 Genes in Two Men With Globozoospermia
Identification Polymorphisms Hrb, GOPC, Csnk2a2 Genes Men Globozoospermia
2008/12/23
Globozoospermia, or round-headed sperm syndrome, is a unique form of male infertility characterized by sperm possessing a round head, lack of an acrosome, and a disorganized midpiece and tail. It ...
Single-Nucleotide Polymorphisms and Mutation Analyses of the TNP1 and TNP2 Genes of Fertile and Infertile Human Male Populations
Protamine transition nuclear protein sperm male infertility genome promoter SNPs
2008/12/23
Previously, we examined the relationship between protamine gene variations and human male infertility. In this study, we show specific variability in the transition nuclear protein genes (TNPs) of...