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  • Title: Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.
    Author: Buttiëns M, Fryns JP, Jonckheere P, Brouckmans-Buttiëns K, Van den Berghe H.
    Journal: Hum Genet; 1985; 71(1):86-8. PubMed ID: 4029956.
    Abstract:
    The association of postaxial polydactyly type A and congenital scalp defect in a 15-year-old severely mentally retarded male confirms the previously reported suggestion that the combination of both anomalies represents a new distinct entity with autosomal dominant inheritance and variable expression.
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