Chromosome 16p12.1 Deletion Syndrome

A condition caused by a 520 kb deletion at 16p12.1. It is characterized by developmental delay, craniofacial dysmorphology and congenital heart defects.

Source: NCI Thesaurus (C129875).

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Chromosome 16p12.1 Deletion Syndrome

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Chromosome 16p12.1 Deletion Syndrome

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