Mapping of partially overlapping de novo deletions across an autism susceptibility region [AUTS5] in two unrelated individuals affected by developmental delays with communication impairment

Autism is a neurodevelopmental disorder characterized by deficits in reciprocal social interaction and communication, and repetitive and stereotyped behaviors and interests. Previous genetic studies of autism have shown evidence of linkage to chromosomes 2q, 3q, 7q, 11p, 16p, and 17q. However, the c...

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Detalles Bibliográficos
Autores principales: Newbury, Dianne F, Warburton, Pamela C, Wilson, Natalie, Bacchelli, Elena, Carone, Simona, Lamb, Janine A, Maestrini, Elena, Volpi, Emanuela V, Mohammed, Shehla, Baird, Gillian, Monaco, Anthony P
Formato: Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680219/
https://www.ncbi.nlm.nih.gov/pubmed/19267418
http://dx.doi.org/10.1002/ajmg.a.32704

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680219/
https://www.ncbi.nlm.nih.gov/pubmed/19267418
http://dx.doi.org/10.1002/ajmg.a.32704

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