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"16p11.2" deletion syndrome
- 16p11.2 deletion syndrome is a disorder caused by a deletion of a small piece of chromosome 16. The deletion ... at a location designated p11.2.People with 16p11.2 deletion syndrome usually have developmental delay and intellectual disability. Most ...
- ... Metay C. Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: a two-hit case with more severe clinical ...
- ... can inherit the chromosomal change. 16p11.2 duplication syndrome 16p11.2 microduplication Autism, susceptibility to, 14B AUTS14B Genetic Testing Registry: Chromosome 16p11.2 duplication syndrome Proximal 16p11.2 microduplication syndrome National Organization for ...
