Title:
Loss of the AZFc region due to a human Y-chromosome microdeletion in infertile male patients

dc.contributor.authorL.K. Pandey
dc.contributor.authorS. Pandey
dc.contributor.authorJ. Gupta
dc.contributor.authorA.K. Saxena
dc.date.accessioned2026-02-07T05:00:26Z
dc.date.issued2010
dc.description.abstractInfertility is a major reproductive health threat; the frequency of male infertility due to Y-chromosome microdeletions is 13-18% in the human population; these microdeletions involve recurrent loss of three non-overlapping regions designated as AZFa, AZFb and AZFc, associated with spermatogenic failure. Several contradictory reports have been published regarding deletion frequency based on sequence-tagged site markers and genotype- phenotype correlation. We examined the prevalence of Yq- deletion in 64 clinically diagnosed infertile male patients. We found a 3% frequency of microdeletion of the AZFc region; hormone profiles (FSH, LH and testosterone) showed significantly (P < 0.001) elevated levels compared to controls. No mutations were observed in the AZFa and AZFb regions, perhaps due to the selective use of sequencetagged site markers. © FUNPEC-RP.
dc.identifier.doi10.4238/vol9-2gmr836
dc.identifier.issn16765680
dc.identifier.urihttps://doi.org/10.4238/vol9-2gmr836
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/22130
dc.publisherFundacao de Pesquisas Cientificas de Ribeirao Preto
dc.subjectAZF regions
dc.subjectMale infertility
dc.subjectSTS markers
dc.subjectY-chromosome microdeletion
dc.titleLoss of the AZFc region due to a human Y-chromosome microdeletion in infertile male patients
dc.typePublication
dspace.entity.typeArticle

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