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Chromosome 16p12.1 Deletion Syndrome
A chromosomal deletion syndrome that is caused by a 520 kb deletion on the short (p) arm of the chromosome at a location designated 16p12.1 and is characterized by developmental delay, craniofacial dysmorphology, and con
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Overview
A chromosomal deletion syndrome that is caused by a 520 kb deletion on the short (p) arm of the chromosome at a location designated 16p12.1 and is characterized by developmental delay, craniofacial dysmorphology, and con
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.