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The Indian Journal of Medical Research|December 1, 1996
Delta F 508 molecular mutation in Indian children with cystic fibrosisM Kabra, M Ghosh, S K Kabra, et al.Pediatric Hematology and Oncology|June 14, 2013
Primary immunodeficiency disorders in the developing world: data from a hospital-based registry in IndiaVasant Chinnabhandar, Satya Prakash Yadav, Dinesh Kaul, et al.The Indian Journal of Medical Research|May 4, 2011
Utility of molecular studies in incontinentia pigmenti patientsSeema Thakur, Ratna D Puri, Sudha Kohli, et al.Indian Pediatrics|October 1, 1995
Clinical and biochemical studies in homocystinuriaM Kaur, M Kabra, G P Das, et al.The Journal of Parasitology|June 1, 1993
Trichuris vulpis infection in an Indian tribal populationS Singh, J C Samantaray, N Singh, et al.Indian Journal of Pediatrics|July 1, 1992
Mixed gonadal dysgenesis and dysgenetic male pseudohermaphroditism--a critical analysisM Rohatgi, D K Gupta, P S Menon, et al.Indian Journal of Pediatrics|June 16, 2001
Congenital myotonic dystrophyS Gulati, M Kabra, S Gera, et al.Genetics and Molecular Research : GMR|July 26, 2013
Prevalence of CYP2C8 polymorphisms in a North Indian populationS Minhas, N Setia, S Pandita, et al.Bulletin of the World Health Organization|January 1, 1992
Dengue haemorrhagic fever in children in DelhiS K Kabra, I C Verma, N K Arora, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|February 28, 2001
Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyR Mathur, P S Menon, M Kabra, et al.Pageof 14