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Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci

BACKGROUND: Congenital heart defects (CHD) is the most common cause of death from a congenital structure abnormality in newborns and is often associated with fetal loss. There are many types of CHD. Human genetic studies have identified genes that are responsible for the inheritance of a particular...

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Detalhes bibliográficos
Main Authors: Flaquer, Antònia, Baumbach, Clemens, Piñero, Estefania, García Algas, Fernando, de la Fuente Sanchez, María Angeles, Rosell, Jordi, Toquero, Jorge, Alonso-Pulpon, Luis, Garcia-Pavia, Pablo, Strauch, Konstantin, Heine-Suñer, Damian
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3664624/
https://ncbi.nlm.nih.gov/pubmed/23705960
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-14-44
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