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Paper Details

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Hum Mol Genet
25
2016
200 kb region, ARNT, CTSK, CTSS, Congenital heart defects, LSL, LSL loci, LSLs, MYH7B, SNPs, Single Nucleotide Polymorphism, birth defects, chromosome 1, chromosome 1q21, chromosome 20, chromosome 20q11, congenital cardiovascular left-sided lesions, congenital heart disease, miR499A, rs12045807, rs3746446, rs6088703
Author NameAffiliation
Neil A Hanchard
Mahshid S Azamian
Jeffrey A TowbinUniversity of Tennessee Health Science Center
Shaine A Morris
William J Dreyer
Susan W Denfield
Henri Justino
Maria R Lantin-Hermoso
Douglas Moodie
Emily J Lawrence
Hugh D Allen
Daniel J Penny
Charles D FraserBaylor College of Medicine
James R Lupski
James R Lupski
Seema R Lalani
Sara M Fitzgerald-ButtDepartment of Pediatrics and Center for Cardiovascular and Pulmonary Research
Peter WhiteDepartment of Pediatrics and Center for Microbial Pathogenesis, Nationwide Children's Hospital
Bernard KeavneyInstitute of Cardiovascular Sciences, The University of Manchester
Suzanne M LealCenter for Statistical Genetics.
Heather J CordellInstitute of Genetic Medicine, Newcastle University
John W Belmont
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