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Article

Bashyam, M.D. and Chaudhary, A.K. and Reddy, E.C. and Radha Rama Devi, A. and Savithri, G.R. and Ratheesh, R. and Bashyam, L. and Mahesh, E. and Sen, D. and Puri, R.D. and Verma, I.C. and Nampoothiri, S. and Vaidyanathan, S. and Chandrashekar, M.D. and Prameela, K. (2010) Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: Identification of novel mutations that affect PAH RNA. Molecular Genetics and Metabolism, 100 (1). pp. 96-99. ISSN 1096-7192

Bashyam, M.D. and Savithri, G.R. and Gopikrishna, M. and Narasimhan, C. (2007) A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family. Canadian Journal of Cardiology, 23 (10). pp. 788-790. ISSN 0828-282X

Radha Rama Devi, A. and Gopikrishna, M. and Ratheesh, R. and Savithri, G.R. and Gowrishankar, S. and Bashyam, M.D. (2006) Farber lipogranulomatosis: clinical and molecular genetic analysis reveals a novel mutation in an Indian family. Journal of Human Genetics, 51 (9). pp. 811-814. ISSN 1434-5161

Bashyam, M.D. and Bashyam, L. and Savithri, G.R. and Gopikrishna, M. and Sangal, V. and Radha Rama Devi, A. (2004) Molecular genetic analyses of beta-thalassemia in South India reveals rare mutations in the beta-globin gene. Journal of Human Genetics, 49 (8). pp. 408-413. ISSN 1434-5161

Bashyam, M.D. and Savithri, G.R. and Kumar, M.S. and Narasimhan, C. and Pratibha, N. (2003) Molecular genetics of familial hypertrophic cardiomyopathy (FHC). Journal of Human Genetics, 48 (2). pp. 55-64. ISSN 1434-5161

Siddiqi, N. and Shamim, M. and Hussain, S. and Choudhary, R.K. and Ahmed, N. and Prachee, and Banerjee, S. and Savithri, G.R. and Alam, M. and Pathak, Niteen and Amin, A. and Hanief, M. and Katoch, V.M. and Sharma, S.K. and Hasnain, S.E. (2002) Molecular characterization of multidrug-resistant isolates of Mycobacterium tuberculosis from patients in North India. Antimicrobial Agents and Chemotherapy, 46 (2). pp. 443-50. ISSN 0066-4804

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