Anubha Sinha

Exostoses, enchondromatosis and metachondromatosis; diagnosis and management.

T. Cole, N. Kiely, R. Freeman, 2016, Acta orthopaedica Belgica.

De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome‐Overlapping Phenotypes

J. Ganesh, I. Krantz, H. Hakonarson, 2015, Human mutation.

De Novo Heterozygous Mutations in SMC 3 Cause a Range of Cornelia de Lange Syndrome-Overlapping Phenotypes Marı́a

J. Ganesh, I. Krantz, H. Hakonarson, 2015 .