Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms

BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is the most common micro-deletion syndrome. The associated 22q11.2 deletion conveys the strongest known molecular risk for schizophrenia. Neurodevelopmental phenotypes, including intellectual disability, are also prominent though variable in severity...

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Detalles Bibliográficos
Autores principales: Guna, Alina, Butcher, Nancy J., Bassett, Anne S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487986/
https://www.ncbi.nlm.nih.gov/pubmed/26137170
http://dx.doi.org/10.1186/s11689-015-9113-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487986/
https://www.ncbi.nlm.nih.gov/pubmed/26137170
http://dx.doi.org/10.1186/s11689-015-9113-x

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