The Impact of CNVs on Outcomes for Infants with Single Ventricle Heart Defects

BACKGROUND: Human genomes harbor copy number variants (CNVs), regions of DNA gains or losses. While pathogenic CNVs are associated with congenital heart disease (CHD), their impact on clinical outcomes is unknown. This study sought to determine whether pathogenic CNVs among infants with single ventr...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Carey, Abigail S., Liang, Li, Edwards, Jonathan, Brandt, Tracy, Mei, Hui, Sharp, Andrew J., Hsu, Daphne T., Newburger, Jane W., Ohye, Richard G., Chung, Wendy K., Russell, Mark W., Rosenfeld, Jill A., Shaffer, Lisa G., Parides, Michael K., Edelmann, Lisa, Gelb, Bruce D.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3987966/
https://ncbi.nlm.nih.gov/pubmed/24021551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.113.000189
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados