Exploring the 7p22.1 Chromosome as a Candidate Region for Autism

A high incidence of de novo chromosomal aberrations in a population of persons with autism suggests a causal relationship between certain chromosomal aberrations and the occurrence of autism. A previous study on a Tunisian boy carrying a t(7;16) translocation identified the 7p22.1 as a positional ca...

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Detalles Bibliográficos
Autores principales: Bayou, Nadia, Belhadj, Ahlem, Daoud, Hussein, Briault, Sylvain, Helayem, M. Bechir, Chaabouni, Habiba, M'rad, Ridha
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856063/
https://www.ncbi.nlm.nih.gov/pubmed/20414355
http://dx.doi.org/10.1155/2010/423894

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856063/
https://www.ncbi.nlm.nih.gov/pubmed/20414355
http://dx.doi.org/10.1155/2010/423894

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