Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies

BACKGROUND: Array comparative genomic hybridization (CGH) has been repeatedly shown to be a successful tool for the identification of genomic variations in a clinical population. During the last decade, the implementation of array CGH has resulted in the identification of new causative submicroscopi...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Iourov, Ivan Y, Vorsanova, Svetlana G, Kurinnaia, Oxana S, Zelenova, Maria A, Silvanovich, Alexandra P, Yurov, Yuri B
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2012
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3547809/
https://ncbi.nlm.nih.gov/pubmed/23272938
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-5-46
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