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Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant
Human Genetics
|January 1, 1985
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.