Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.

Congenital conotruncal cardiac defects occur with increased frequency in patients with DiGeorge syndrome (DGS). Previous studies have shown that the majority of patients with DGS or velocardiofacial syndrome (VCFS) have a microdeletion within chromosomal region 22q11. We hypothesised that patients w...

ver descrição completa

Detalhes bibliográficos

Publicado no:	J Med Genet
Principais autores:	Goldmuntz, E, Driscoll, D, Budarf, M L, Zackai, E H, McDonald-McGinn, D M, Biegel, J A, Emanuel, B S
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMJ Publishing Group 1993
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016559/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7901419/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.10.807
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!