Copy number variants prioritization after array-CGH analysis – a cohort of 1000 patients

BACKGROUND: Array-based comparative genomic hybridization has been assumed to be the first genetic test offered to detect genomic imbalances in patients with unexplained intellectual disability with or without dysmorphisms, multiple congenital anomalies, learning difficulties and autism spectrum dis...

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Detalles Bibliográficos
Autores principales: Carreira, Isabel Marques, Ferreira, Susana Isabel, Matoso, Eunice, Pires, Luís Miguel, Ferrão, José, Jardim, Ana, Mascarenhas, Alexandra, Pinto, Marta, Lavoura, Nuno, Pais, Cláudia, Paiva, Patrícia, Simões, Lúcia, Caramelo, Francisco, Ramos, Lina, Venâncio, Margarida, Ramos, Fabiana, Beleza, Ana, Sá, Joaquim, Saraiva, Jorge, de Melo, Joana Barbosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696247/
https://www.ncbi.nlm.nih.gov/pubmed/26719768
http://dx.doi.org/10.1186/s13039-015-0202-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696247/
https://www.ncbi.nlm.nih.gov/pubmed/26719768
http://dx.doi.org/10.1186/s13039-015-0202-z

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