Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

Detalles Bibliográficos
Autores principales: Newbury, Dianne F, Mari, Francesca, Sadighi Akha, Elham, MacDermot, Kay D, Canitano, Roberto, Monaco, Anthony P, Taylor, Jenny C, Renieri, Alessandra, Fisher, Simon E, Knight, Samantha J L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598310/
https://www.ncbi.nlm.nih.gov/pubmed/22909776
http://dx.doi.org/10.1038/ejhg.2012.166

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598310/
https://www.ncbi.nlm.nih.gov/pubmed/22909776
http://dx.doi.org/10.1038/ejhg.2012.166

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