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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 ...
- ... structure or number of copies of chromosome 16. 16p11.2 deletion syndrome is caused by a deletion of about 600, ... the missing genes contribute to the features of 16p11.2 deletion syndrome, which include delayed development; intellectual disability; and autism ...
- Developmental Disabilities (National Library of Medicine)Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disabilities. ...
- Autism Spectrum Disorder (National Library of Medicine)Autism spectrum disorder (ASD) is a neurological and developmental disorder that begins early in childhood and lasts throughout a person's life. It affects how ...
- ... 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 ...
