Evidence for Involvement of GNB1L in Autism

Structural variations in the chromosome 22q11.2 region mediated by nonallelic homologous recombination result in 22q11.2 deletion (del22q11.2) and 22q11.2 duplication (dup22q11.2) syndromes. The majority of del22q11.2 cases have facial and cardiac malformations, immunologic impairments, specific cog...

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Detalles Bibliográficos
Autores principales: Chen, Ying-Zhang, Matsushita, Mark, Girirajan, Santhosh, Lisowski, Mark, Sun, Elizabeth, Sul, Youngmee, Bernier, Raphael, Estes, Annette, Dawson, Geraldine, Minshew, Nancy, Shellenberg, Gerard D, Eichler, Evan E, Rieder, Mark J, Nickerson, Deborah A, Tsuang, Debby W, Tsuang, Ming T, Wijsman, Ellen M, Raskind, Wendy H, Brkanac, Zoran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2012
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270696/
https://www.ncbi.nlm.nih.gov/pubmed/22095694
http://dx.doi.org/10.1002/ajmg.b.32002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270696/
https://www.ncbi.nlm.nih.gov/pubmed/22095694
http://dx.doi.org/10.1002/ajmg.b.32002

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