Prader–Willi syndrome and autism spectrum disorders: an evolving story

Prader–Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11–q13, individuals with PWS have mild to moderate intellectual disabilities, repetitive and compulsive behaviors, skin picking, tantrums,...

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Detalles Bibliográficos
Autores principales: Dykens, Elisabeth M., Lee, Evon, Roof, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261277/
https://www.ncbi.nlm.nih.gov/pubmed/21858456
http://dx.doi.org/10.1007/s11689-011-9092-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261277/
https://www.ncbi.nlm.nih.gov/pubmed/21858456
http://dx.doi.org/10.1007/s11689-011-9092-5

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