Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders

Copy number variants (CNVs) at chromosome 16p13.11 have been associated with a range of neurodevelopmental disorders including autism, ADHD, intellectual disability and schizophrenia. Significant sex differences in prevalence, course and severity have been described for a number of these conditions...

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Detalles Bibliográficos
Autores principales: Tropeano, Maria, Ahn, Joo Wook, Dobson, Richard J. B., Breen, Gerome, Rucker, James, Dixit, Abhishek, Pal, Deb K., McGuffin, Peter, Farmer, Anne, White, Peter S., Andrieux, Joris, Vassos, Evangelos, Ogilvie, Caroline Mackie, Curran, Sarah, Collier, David A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630198/
https://www.ncbi.nlm.nih.gov/pubmed/23637818
http://dx.doi.org/10.1371/journal.pone.0061365

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630198/
https://www.ncbi.nlm.nih.gov/pubmed/23637818
http://dx.doi.org/10.1371/journal.pone.0061365

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