Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference37 articles.
1. REVIEW: Embryological observations on the female genital tract
2. Congenital Bilateral Absence of the Vas Deferens
3. Congenital absence of the uterus and vagina (CAUV) is not associated with the N314D allele of the Galactose-1-Phosphate Uridyl Transferase (GALT) gene
4. Heritable aspects of uterine anomalies. II. Genetic analysis of Müllerian aplasia**Supported in part by grants from the March of Dimes Birth Defects Foundation and by NIH grants HD 11021 and HD 02841.
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