Associated Papers
SOX7 loss-of-function variation as a cause of familial congenital heart disease.
Huang RT et al.
American Journal of Translational Research, 2022
Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.
Cohen ASA et al.
American Journal of Medical Genetics. Part A, 2020
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
Sun YM et al.
G3 (bethesda, Md.), 2016
Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Töpf A et al.
Plos One, 2014
Chromosome 4q deletion syndrome: narrowing the cardiovascular critical region to 4q32.2-q34.3.
Xu W et al.
American Journal of Medical Genetics. Part A, 2012
Transcription factor HAND2 mutations in sporadic Chinese patients with congenital heart disease.
Shen L et al.
Chinese Medical Journal, 2010
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