Associated Papers
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Al Turki S et al.
American Journal of Human Genetics, 2016
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy.
Poulter JA et al.
American Journal of Human Genetics, 2016
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
Poulter JA et al.
American Journal of Human Genetics, 2010
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