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Article

Single-nucleotide variant in multiple copies of a deleted in azoospermia (DAZ) sequence - a human Y chromosome quantitative polymorphism.

Human heredity - 1 Jan 2002

Szmulewicz Martin N, Ruiz Luis M, Reategui Erika P, Hussini Saeed, Herrera Rene J

Abstract excerpt

The evolution of the deleted in azoospermia (DAZ) gene family supports prevalent theories on the origin and development of sex chromosomes and sexual dimorphism. The ancestral DAZL gene in human chromosome 3 is known to be involved in germline development of both males and females. The available phylogenetic data suggest that some time after the divergence of the New World and Old World monkey lineages, the DAZL...

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Source

Identifiers

PMID: 11901266
DOI: 10.1159/000048599

Genes

DAZL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Single-nucleotide variant in multiple copies of a deleted in azoospermia (DAZ) sequence - a human Y chromosome quantitative polymorphism.PMID 11901266Read ↗

Single-nucleotide polymorphism in repetitive sequences of the human deleted in azoospermia complex.Semantic proximity Read ↗

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Variants in Deleted in AZoospermia-Like (DAZL) are correlated with reproductive parameters in men and women.Semantic proximity Read ↗

The human DAZ genes, a putative male infertility factor on the Y chromosome, are highly polymorphic in the DAZ repeat regions.Semantic proximity Read ↗

Evolution of the Japanese Y chromosome by analysis of the haplogroups and the deletion of the gene in the AZFc region.Semantic proximity Read ↗

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