TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy
Manal Alaamery(King Abdulaziz City for Science and Technology), Alex V. Postma(Amsterdam University Medical Centers)
Cited by 1
Related Papers
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
|Circulation Research|2019|198
Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly
|Circulation Cardiovascular Genetics|2010|187
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
|Nature Genetics|2013|165
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot
|Human Molecular Genetics|2013|109