Associated Papers
Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.
He Q et al.
Advanced Science (weinheim, Baden-wurttemberg, Germany), 2025
40464334 (PubMed )
Supplement: ADVS-12-e12073-s004.xlsx › Sheet1
A Novel Variant in the Cyto-Tail of SMO Gene Underlying Isolated Postaxial Polydactyly.
Javed Khan M et al.
Molecular Syndromology, 2024
Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO).
Fan L et al.
Frontiers in Genetics, 2022
Compound heterozygous mutations in SMO associated with anterior segment dysgenesis and morning glory syndrome.
Zhang J et al.
Gene, 2019
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