Persistent Truncus Arteriosus
Last Posted: Jun 02, 2014
- Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects.
Wang Xike, et al. Molecular medicine reports 2014 8 (2) 743-8
- Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.
Xiong Fu, et al. Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 0 0 (2) 141-5
- Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.
Guo Tingwei, et al. Human mutation 2011 11 (11) 1278-89
- Persistent truncus arteriosus
From NCATS Genetic and Rare Diseases Information Center
- A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.
Lin Xiaoping, et al. Journal of human genetics 2010 10 (10) 662-7
- Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases.
Lee Chien-Nan, et al. Acta obstetricia et gynecologica Scandinavica 2005 12 (12) 1134-40
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