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
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
Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome.
McElreavey K et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2020
Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis Spectrum.
da Silva TE et al.
The Journal of Clinical Endocrinology and Metabolism, 2019
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