Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications

Microdeletions and microduplications encompassing a ~593-kb region of 16p11.2 have been implicated as one of the most common genetic causes of susceptibility to autism/autism spectrum disorder (ASD). We report 45 microdeletions and 32 microduplications of 16p11.2, representing 0.78% of 9,773 individ...

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Detalles Bibliográficos
Autores principales: Rosenfeld, Jill A., Coppinger, Justine, Bejjani, Bassem A., Girirajan, Santhosh, Eichler, Evan E., Shaffer, Lisa G., Ballif, Blake C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125720/
https://www.ncbi.nlm.nih.gov/pubmed/21731881
http://dx.doi.org/10.1007/s11689-009-9037-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125720/
https://www.ncbi.nlm.nih.gov/pubmed/21731881
http://dx.doi.org/10.1007/s11689-009-9037-4

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