Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAE genes in a family with developmental delay and behavioural problems

BACKGROUND: Deletions and duplications of the PAFAH1B1 and YWHAE genes in 17p13.3 are associated with different clinical phenotypes. In particular, deletion of PAFAH1B1 causes isolated lissencephaly while deletions involving both PAFAH1B1 and YWHAE cause Miller-Dieker syndrome. Isolated duplications...

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Detalles Bibliográficos
Autores principales: Capra, Valeria, Mirabelli-Badenier, Marisol, Stagnaro, Michela, Rossi, Andrea, Tassano, Elisa, Gimelli, Stefania, Gimelli, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495055/
https://www.ncbi.nlm.nih.gov/pubmed/23035971
http://dx.doi.org/10.1186/1471-2350-13-93

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495055/
https://www.ncbi.nlm.nih.gov/pubmed/23035971
http://dx.doi.org/10.1186/1471-2350-13-93

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