Associated Papers
Molecular Diagnosis of 46,XY Disorders of Sex Development: An Efficient Initial Molecular Analysis Using a Custom-Designed Targeted Gene Panel in a Single-Center Study.
Poyrazoglu S et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2026
A Novel Mutation in the Androgen Receptor Gene of Female Patients with 46,XY Karyotype.
Uslu IN et al.
Current Issues in Molecular Biology, 2025
Analysis of genetic and clinical characteristics of androgen insensitivity syndrome: a cohort study including 12 families.
Yuan Z et al.
European Journal of Endocrinology, 2024
The genetic spectrum of a Chinese series of patients with 46, XY disorders of the sex development.
Zhang W et al.
Andrology, 2024
Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort
Touzon MS et al.
Journal of Clinical Research in Pediatric Endocrinology, 2019
Correlation of androgen receptor and SRD5A2 gene mutations with pediatric hypospadias in 46, XY DSD children.
Fu XH et al.
Genetics and Molecular Research : Gmr, 2016
Loss of heterozygosity: what is it good for?
Ryland GL et al.
Bmc Medical Genomics, 2015
26231170 (PubMed )
Supplement: 12920_2015_123_MOESM2_ESM.xlsx › NewSuppTable4
AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.
Akcay T et al.
Andrology, 2014
Androgen insensitivity syndrome.
Hughes IA et al.
Seminars in Reproductive Medicine, 2012
Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.
Yuan SM et al.
Asian Journal of Andrology, 0
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