Associated Papers
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_S3._Additional_findings_obtained_by_WES_after_specific_filtering.pdf
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 19.19
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