Items where Author is "Faruq, M."

Faruq, M. ; Narang, A. ; Kumari, R. ; Pandey, R. ; Garg, A. ; Behari, M. ; Dash, D. ; Srivastava, A. K. ; Mukerji, M. (2014) Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families Clinical Genetics, 86 (4). pp. 335-341. ISSN 0009-9163

Yadav, R. ; Sharma, M. C. ; Malgulwar, P. B. ; Pathak, P. ; Sigamani, E. ; Suri, V. ; Sarkar, C. ; Kumar, A. ; Singh, M. ; Sharma, B. S. ; Garg, A. ; Bakhshi, S. ; Faruq, M. (2014) Prognostic value of MIB-1, p53, epidermal growth factor receptor, and INI1 in childhood chordomas Neuro-Oncology, 16 (3). pp. 372-381. ISSN 1522-8517

Faruq, M. ; Narang, A. ; Kumari, R. ; Dash, D. ; Srivastava, A. K. ; Mukerji, M. (2013) Genetic deconvolution of cerebellar ataxias in India through next generation sequencing: Novel mutations in atypical and typical genetic loci Journal of the Neurological Sciences, 333 . e142. ISSN 0022-510X

Srivastava, A. K. ; Faruq, M. ; Shakya, S. ; Negi, P. ; Kumar, D. ; Kumar, N. ; Goyal, V. ; Mukerji, M. ; Behari, M. (2013) Reduced penetrance alleles of TBP (SCA17) in Indian ataxia cohort: Homozygous mutation and ambiguity of 41–/INS;44 CAG/CAA for pathogenic association Journal of the Neurological Sciences, 333 . e69. ISSN 0022-510X

Srivastava, A. K. ; Faruq, M. ; Dada, T. ; Garg, A. ; Singh, S. ; Mukerji, M. ; Behari, M. (2013) Spinocerebellar ataxia 7 (sca7) in India: Genotype–/INS;phenotype correlation and insight into origin of mutation in a predisposed endogamous population Journal of the Neurological Sciences, 333 (Suppl1). e107. ISSN 0022-510X