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Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly
A syndrome characterized by congenital heart defects, hamartomas of tongue, and polysyndactyly that is caused by homozygous or compound heterozygous mutation in the WDPCP gene on chromosome 2p15.
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Overview
A syndrome characterized by congenital heart defects, hamartomas of tongue, and polysyndactyly that is caused by homozygous or compound heterozygous mutation in the WDPCP gene on chromosome 2p15.
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