Associated Papers
Profile of DHX37 gene defects in human genetic diseases: 46,XY disorders of sex development.
Peng H et al.
Frontiers in Endocrinology, 2025
Identification and functional analysis of a rare variant of gene DHX37 in a patient with 46,XY disorders of sex development.
Jiang W et al.
Molecular Genetics & Genomic Medicine, 2024
DHX37 and the Implications in Disorders of Sex Development: An Update Review.
de Oliveira FR et al.
Hormone Research in Paediatrics, 2024
Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants.
Jiali C et al.
Frontiers in Genetics, 2024
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.
de Oliveira FR et al.
Life (basel, Switzerland), 2023
37240737 (PubMed )
Supplement: life-13-01093-s001.zip › Table_S1._Variants_described_so_far_in_published_articles.pdf
Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development.
Gomes NL et al.
The Journal of Clinical Endocrinology and Metabolism, 2022
Variants in 46,XY DSD-Related Genes in Syndromic and Non-Syndromic Small for Gestational Age Children with Hypospadias.
Leitao Braga B et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2022
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