L. Molinari

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

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

Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions

J. Belmont, J. Towbin, S. Lalani, 2003, American journal of medical genetics. Part A.

PTPN11 Mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13

R. Gibbs, J. Belmont, F. Yu, 2002, Human mutation.

SNP genotyping to screen for a common deletion in CHARGE Syndrome

J. Belmont, J. Towbin, S. Lalani, 2005, BMC Medical Genetics.

SEMA3E mutation in a patient with CHARGE syndrome

S. Lalani, S. Fernbach, D. M. Martin, 2004, Journal of Medical Genetics.

Low Levels of Genetic Divergence across Geographically and Linguistically Diverse Populations from India

Noah A Rosenberg, Madhuri Hegde, J. Weber, 2006, PLoS genetics.

A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductase.

J. Belmont, J. Towbin, S. Fernbach, 2004, Birth defects research. Part A, Clinical and molecular teratology.