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Article

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

BMC medical genetics - 12 Jul 2014

Uwineza Annette, Caberg Jean-Hubert, Hitayezu Janvier, Hellin Anne Cecile, Jamar Mauricette, Dideberg Vinciane, Rusingiza Emmanuel K, Bours Vincent, Mutesa Leon

Abstract excerpt

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 comparative genomic hybridization was performed in 50 Rwandan patients with development delay/intellectual disability and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 25016475
DOI: 10.1186/1471-2350-15-79
PMCID: PMC4123504

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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