Associated Papers
Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome.
Zhian S et al.
American Journal of Medical Genetics. Part A, 2012
Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population.
Li H et al.
Circulation. Cardiovascular Genetics, 2012
A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India.
Kusuma L et al.
Genetic Testing and Molecular Biomarkers, 0
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