Associated Papers
SMAD6 variants in craniosynostosis: genotype and phenotype evaluation.
Calpena E et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2020
32499606 (PubMed )
Supplement: 41436_2020_817_MOESM5_ESM.xlsx › Table_S4
SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.
Yang Y et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
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