Associated Papers
A Novel ZBTB20 Variant in a Patient with Primrose Syndrome: A Rare Clinical Entity with Distinctive Features.
Soğukpınar M et al.
Molecular Syndromology, 2024
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis.
Hyder Z et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
34429528 (PubMed )
Supplement: EMS138012-supplement-Table_S3.xlsx › Sheet1
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