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
Case Report: De novo DHX37 mutations in Saudi patients with 46,XY differences of sex development.
Alabduljabbar A 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
A novel DEAH-box helicase 37 mutation associated with differences of sex development.
Wan Y et al.
Frontiers in Endocrinology, 2023
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37.
Zidoune H et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2021
Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD.
Buonocore F et al.
Journal of the Endocrine Society, 2019
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