M. Gopikrishna

Farber lipogranulomatosis: clinical and molecular genetic analysis reveals a novel mutation in an Indian family

M. Bashyam, R. Ratheesh, A. Devi, 2006, Journal of Human Genetics.

Molecular genetic analyses of β-thalassemia in South India reveals rare mutations in the β-globin gene

M. Bashyam, V. Sangal, L. Bashyam, 2004, Journal of Human Genetics.

Molecular genetic analyses of beta-thalassemia in South India reveals rare mutations in the beta-globin gene.

M. Bashyam, V. Sangal, L. Bashyam, 2004, Journal of human genetics.

A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family.

M. Bashyam, C. Narasimhan, G. Savithri, 2007, The Canadian journal of cardiology.