Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients

BACKGROUND: Chromosomal microarray analysis (CMA) is currently the most widely adopted clinical test for patients with unexplained intellectual disability (ID), developmental delay (DD), and congenital anomalies. Its use has revealed the capacity to detect copy number variants (CNVs), as well as reg...

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Detalles Bibliográficos
Autores principales: Choucair, Nancy, Ghoch, Joelle Abou, Corbani, Sandra, Cacciagli, Pierre, Mignon-Ravix, Cecile, Salem, Nabiha, Jalkh, Nadine, El Sabbagh, Sandra, Fawaz, Ali, Ibrahim, Tony, Villard, Laurent, Mégarbané, André, Chouery, Eliane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411788/
https://www.ncbi.nlm.nih.gov/pubmed/25922617
http://dx.doi.org/10.1186/s13039-015-0130-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411788/
https://www.ncbi.nlm.nih.gov/pubmed/25922617
http://dx.doi.org/10.1186/s13039-015-0130-y

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