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Article

HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina.

Gene - 15 Apr 2013

Ekici Arif B, Strissel Pamela L, Oppelt Patricia G, Renner Stefan P, Brucker Sara, Beckmann Matthias W, Strick Reiner

Abstract excerpt

Congenital genital malformations occurring in the female population are estimated to be 5 per 1000 and associate with infertility, abortion, stillbirth, preterm delivery and other organ abnormalities. Complete aplasia of the uterus, cervix and upper vagina (Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome) has an incidence of 1 per 4000 female live births. The molecular etiology of congenital genital malformations...

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Source

Identifiers

PMID: 23376215
DOI: 10.1016/j.gene.2013.01.030

Genes

HOXA10
HOXA13

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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