Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects

The goal of this study was to identify the contribution of common genetic variants to Down syndrome−associated atrioventricular septal defect, a severe heart abnormality. Compared with the euploid population, infants with Down syndrome, or trisomy 21, have a 2000-fold increased risk of presenting wi...

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Detalhes bibliográficos
Publicado no:G3 (Bethesda)
Main Authors: Ramachandran, Dhanya, Zeng, Zhen, Locke, Adam E., Mulle, Jennifer G., Bean, Lora J.H., Rosser, Tracie C., Dooley, Kenneth J., Cua, Clifford L., Capone, George T., Reeves, Roger H., Maslen, Cheryl L., Cutler, David J., Feingold, Eleanor, Sherman, Stephanie L., Zwick, Michael E.
Formato: Artigo
Idioma:Inglês
Publicado em: Genetics Society of America 2015
Assuntos:
Investigations
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4592978/
https://ncbi.nlm.nih.gov/pubmed/26194203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.115.019943
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