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 beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Uwineza, Annette, Caberg, Jean-Hubert, Hitayezu, Janvier, Hellin, Anne Cecile, Jamar, Mauricette, Dideberg, Vinciane, Rusingiza, Emmanuel K, Bours, Vincent, Mutesa, Leon
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2014
Ämnen:
Research Article
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk