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Chromosome 16p11.2 Deletion Syndrome, 220-Kb
A chromosomal deletion syndrome that is characterized by developmental delay, mild intellectual disability and autism spectrum disorder and that is caused by a partial deletion of the short arm of chromosome 16, specific
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Overview
A chromosomal deletion syndrome that is characterized by developmental delay, mild intellectual disability and autism spectrum disorder and that is caused by a partial deletion of the short arm of chromosome 16, specific
Resources
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Talk with people who understand, share what helps, and find support from others living with chromosome 16p11.2 deletion syndrome, 220-kb. Private, moderated, and free.
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