G. Savithri

Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNA.

M. Bashyam, S. Nampoothiri, I. Verma, 2010, Molecular genetics and metabolism.

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.

Molecular Characterization of Multidrug-Resistant Isolates of Mycobacterium tuberculosis from Patients in North India

N. Ahmed, S. Hasnain, N. Pathak, 2002, Antimicrobial Agents and Chemotherapy.

Molecular genetics of familial hypertrophic cardiomyopathy (FHC)

M. Bashyam, P. Nallari, C. Narasimhan, 2003, 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.