Items where Author is "Saleem, Q."

Saleem, Q. ; Roy, S. ; Murgood, U. ; Saxena, R. ; Verma, I. C. ; Anand, A. ; Muthane, U. ; Jain, S. ; Brahmachari, S. K. (2003) Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population Acta Neurologica Scandinavica, 108 (4). pp. 281-286. ISSN 0001-6314

Mukherjee, O. ; Saleem, Q. ; Purushottam, M. ; Anand, A. ; Brahmachari, S. K. ; Jain, S. (2002) Common psychiatric diseases and human genetic variation Community Genetics, 5 (3). pp. 171-177. ISSN 1422-2795

Saleem, Q. ; Dash, D. ; Gandhi, C. ; Kishore, A. ; Benegal, V. ; Sherrin, T. ; Mukherjee, O. ; Jain, S. ; Brahmachari, S. K. (2001) Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder Molecular Psychiatry, 6 (6). pp. 694-700. ISSN 1359-4184

Saleem, Q. ; Ganesh, S. ; Vijaykumar, M. ; Reddy, Y. C. J. ; Brahmachari, S. K. ; Jain, Sanjeev (2000) Association analysis of 5HT transporter gene in bipolar disorder in the Indian population American Journal of Medical Genetics, 96 (2). pp. 170-172. ISSN 0148-7299

Mukerji, M. ; Choudhry, S. ; Saleem, Q. ; Padma, M. V. ; Maheshwari, M. C. ; Jain, S. (2000) Molecular analysis of Friedreich's ataxia locus in the Indian population Acta Neurologica Scandinavica, 102 (4). pp. 227-229. ISSN 0001-6314

Saleem, Q. ; Choudhry, S. ; Mukerji, M. ; Bashyam, L. ; Padma, M. V. ; Chakravarthy, A. ; Maheshwari, M. C. ; Jain, S. ; Brahmachari, S. K. (2000) Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation Human Genetics, 106 (2). pp. 179-187. ISSN 0340-6717

Gourie-Devi, M. ; Chaudhuri, J. R. ; Vasanth, A. ; Saleem, Q. ; Mutsuddi, M. ; Gopinath, M. ; Sarkar, P. S. ; Brahmachari, S. K. (1988) Correlation of clinical profile of myotonic dystrophy with CTG repeats in the myotonin protein kinase gene Indian Journal of Medical Research, 107 . pp. 187-196. ISSN 0971-5916