X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation

BACKGROUND: Aproximately 5–10% of cases of mental retardation in males are due to copy number variations (CNV) on the X chromosome. Novel technologies, such as array comparative genomic hybridization (aCGH), may help to uncover cryptic rearrangements in X-linked mental retardation (XLMR) patients. W...

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Detalles Bibliográficos
Autores principales: Madrigal, I, Rodríguez-Revenga, L, Armengol, L, González, E, Rodriguez, B, Badenas, C, Sánchez, A, Martínez, F, Guitart, M, Fernández, I, Arranz, JA, Tejada, MI, Pérez-Jurado, LA, Estivill, X, Milà, M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234261/
https://www.ncbi.nlm.nih.gov/pubmed/18047645
http://dx.doi.org/10.1186/1471-2164-8-443

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234261/
https://www.ncbi.nlm.nih.gov/pubmed/18047645
http://dx.doi.org/10.1186/1471-2164-8-443

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