Article

Das Bhowmik, A. and Karthik, T. and Uppin, M. and Sundaram, C. and Dalal, Ashwin (2018) Targeted next generation sequencing reveals novel splice site mutations in COL6A3 gene in a patient with congenital muscular dystrophy. Neurology India, 66 (6). pp. 1812-1814. ISSN 0028-3886

Das Bhowmik, A. and Dalal, Ashwin and Matta, D. and Sundaram, C. and Aggarwal, Shagun (2016) Targeted Next Generation Sequencing Identifies a Novel Deletion in LAMA2 Gene in a Merosin Deficient Congenital Muscular Dystrophy Patient. Indian Journal of Pediatrics, 83 (4). pp. 354-355. ISSN 0019-5456

Ramaswamy, P. and Viswakalyan, K. and Gowrishankar, S. and Mohana Vamsy, C. and Patnaik, S. and Uppin, S.G. and Rao, S. and Raju, K.N. and Sastry, R.A. and Sundaram, C. and Srinivasulu, M. and Anjayneyulu, V. and Bashyam, M.D. (2013) Distinct genetic aberrations in oesophageal adeno and squamous carcinoma. European Journal of Clinical Investigation, 43 (12). pp. 1233-1239. ISSN 0014-2972

Khursheed, M. and Kolla, J.N. and Kotapalli, V. and Gupta, N. and Gowrishankar, S. and Uppin, S.G. and Sastry, R.A. and Koganti, S. and Sundaram, C. and Pollack, J.R. and Bashyam, M.D. (2013) ARID1B, a member of the human SWI/SNF chromatin remodeling complex, exhibits tumour-suppressor activities in pancreatic cancer cell lines. British Journal of Cancer, 108 (10). pp. 2056-2062. ISSN 0007-0920