Liana Smith

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.

J. Belmont, J. Towbin, S. Fernbach, 2009, Human molecular genetics.

Danon Disease as an Underrecognized Cause of Hypertrophic Cardiomyopathy in Children

J. Towbin, S. Fernbach, W. Dreyer, 2005, Circulation.