Exome Analysis of a Family with Pleiotropic Congenital Heart Disease

BACKGROUND: A number of single gene defects have been identified in patients with isolated or nonsyndromic congenital heart defects (CHD). However, due to significant genetic heterogeneity candidate gene approaches have had limited success in finding high-risk alleles in most cases. OBJECTIVE: Use e...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Arrington, Cammon B., Bleyl, Steven B., Matsunami, Norisada, Bonnell, Gabriel D., Otterud, Brith E.M., Nielsen, Douglas C., Stevens, Jeffrey, Levy, Shawn, Leppert, Mark F., Bowles, Neil E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3329568/
https://ncbi.nlm.nih.gov/pubmed/22337856
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.111.961797
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados