S. Banerjee-Basu

Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans.

A. Schier, J. Belmont, J. Towbin, 2007, American journal of human genetics.

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.

J. Belmont, J. Towbin, A. Baxevanis, 2009, Molecular genetics and metabolism.