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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:G3 (Bethesda)
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Genetics Society of America 2015
Témata:
Investigations
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky