Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

BACKGROUND: Array-CGH is considered as the first-tier investigation used to identify copy number variations. Right now, there is no available data about the genetic etiology of patients with development delay/intellectual disability and congenital malformation in East Africa. METHODS: Array comparat...

Full description

Saved in:

Bibliographic Details
Main Authors:	Uwineza, Annette, Caberg, Jean-Hubert, Hitayezu, Janvier, Hellin, Anne Cecile, Jamar, Mauricette, Dideberg, Vinciane, Rusingiza, Emmanuel K, Bours, Vincent, Mutesa, Leon
Format:	Artigo
Language:	Inglês
Published:	BioMed Central 2014
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4123504/ https://ncbi.nlm.nih.gov/pubmed/25016475 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-79
Tags:	Add Tag No Tags, Be the first to tag this record!

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

Similar Items