Abstract
Objective To identify single-nucleotide polymorphisms (SNPs) in specific candidate genes associated with patent ductus arteriosus in term infants. Study design We conducted an initial family-based, candidate gene study to analyze genotype data from DNA samples obtained from 171 term infants and their parents enrolled in the National Birth Defects Prevention Study (NBDPS). We performed transmission disequilibrium testing (TDT) using a panel of 55 SNPs in 17 genes. Replication of SNPs with P
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Patel, P. M., Momany, A. M., Schaa, K. L., Romitti, P. A., Druschel, C., Cooper, M. E., … Dagle, J. M. (2016). Genetic Modifiers of Patent Ductus Arteriosus in Term Infants. Journal of Pediatrics, 176, 57-61.e1. https://doi.org/10.1016/j.jpeds.2016.05.066
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