The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

BACKGROUND: Chromosomal microarray analysis has been shown to be a valuable and cost effective assay for elucidating copy number variants (CNVs) in children with intellectual disability and developmental delay (ID/DD). METHODS: In our study, we performed array-based comparative genomic hybridization...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:BMC Med Genomics
Autores principales: Wayhelova, Marketa, Smetana, Jan, Vallova, Vladimira, Hladilkova, Eva, Filkova, Hana, Hanakova, Marta, Vilemova, Marcela, Nikolova, Petra, Gromesova, Barbora, Gaillyova, Renata, Kuglik, Petr
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6651926/
https://ncbi.nlm.nih.gov/pubmed/31337399
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-019-0559-7
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares