An atypical autistic phenotype associated with a 2q13 microdeletion: a case report

BACKGROUND: Autism spectrum disorders are serious neurodevelopmental disorders that affect approximately 1% of the population. These disorders are substantially influenced by genetics. Several recent linkage analyses have examined copy number variations associated with autism risk. Microdeletion of...

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Detalles Bibliográficos
Autores principales: Guivarch, Jokthan, Chatel, Clarisse, Mortreux, Jeremie, Missirian, Chantal, Philip, Nicole, Poinso, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857311/
https://www.ncbi.nlm.nih.gov/pubmed/29549886
http://dx.doi.org/10.1186/s13256-018-1620-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857311/
https://www.ncbi.nlm.nih.gov/pubmed/29549886
http://dx.doi.org/10.1186/s13256-018-1620-4

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