Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

BACKGROUND: Ventricular septal defects (VSDs) constitute the most prevalent congenital heart disease (CHD), occurs either in isolation (isolated VSD) or in combination with other cardiac defects (complex VSD). Copy number variation (CNV) has been highlighted as a possible contributing factor to the...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:BMC Med Genomics
Hlavní autoři: An, Yu, Duan, Wenyuan, Huang, Guoying, Chen, Xiaoli, Li, Li, Nie, Chenxia, Hou, Jia, Gui, Yonghao, Wu, Yiming, Zhang, Feng, Shen, Yiping, Wu, Bailin, Wang, Hongyan
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4705616/
https://ncbi.nlm.nih.gov/pubmed/26742958
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-015-0163-4
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky