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
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
Sun YM et al.
G3 (bethesda, Md.), 2016
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
Hand factors as regulators of cardiac morphogenesis and implications for congenital heart defects.
Vincentz JW et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2011
Transcription factor HAND2 mutations in sporadic Chinese patients with congenital heart disease.
Shen L et al.
Chinese Medical Journal, 2010
Select a paper to view details