Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Nat Genet
; 49(11): 1593-1601, 2017 Nov.
Article
in En
| MEDLINE
| ID: mdl-28991257
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Autistic Disorder
/
Myosin Heavy Chains
/
Genetic Predisposition to Disease
/
Cardiac Myosins
/
Vascular Endothelial Growth Factor Receptor-3
/
Growth Differentiation Factor 1
/
Heart Defects, Congenital
Type of study:
Etiology_studies
/
Observational_studies
/
Risk_factors_studies
Limits:
Adult
/
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
Nat Genet
Journal subject:
GENETICA MEDICA
Year:
2017
Document type:
Article
Affiliation country:
Estados Unidos
Country of publication:
Estados Unidos