A genetic association study detects haplotypes associated with obstructive heart defects

The development of congenital heart defects (CHDs) involves a complex interplay between genetic variants, epigenetic variants, and environmental exposures. Previous studies have suggested that susceptibility to CHDs is associated with maternal genotypes, fetal genotypes, and maternal–fetal genotype...

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Udgivet i:Hum Genet
Main Authors: Li, Ming, Cleves, Mario A., Mallick, Himel, Erickson, Stephen W., Tang, Xinyu, Nick, Todd G., Macleod, Stewart L., Hobbs, Charlotte A.
Format: Artigo
Sprog:Inglês
Udgivet: 2014
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4313870/
https://ncbi.nlm.nih.gov/pubmed/24894164
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-014-1453-1
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