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Page 1
Denys-Drash syndrome.
Suri M, Kabra M, Kataria A, Singh GR, Sharma S, Gupta AK, Menon PS, Verma IC. Suri M, et al. Among authors: verma ic. Indian Pediatr. 1995 Dec;32(12):1310-3. Indian Pediatr. 1995. PMID: 8772891 No abstract available.
Clinical and enzyme studies in Gaucher disease.
Kaur M, Kabra M, Kher A, Naik G, Bharucha BA, Verma IC. Kaur M, et al. Among authors: verma ic. Indian Pediatr. 1996 Sep;33(9):735-8. Indian Pediatr. 1996. PMID: 9057400
Dysmorphology diagnosis.
Puri RD, Verma IC. Puri RD, et al. Among authors: verma ic. Indian J Pediatr. 2004 Jun;71(6):535-9. doi: 10.1007/BF02724297. Indian J Pediatr. 2004. PMID: 15226565
Spectrum of severe skeletal dysplasias in North India.
Puri RD, Thakur S, Verma IC. Puri RD, et al. Among authors: verma ic. Indian J Pediatr. 2007 Nov;74(11):995-1002. doi: 10.1007/s12098-007-0183-y. Indian J Pediatr. 2007. PMID: 18057679
Molecular studies of achondroplasia.
Nahar R, Saxena R, Kohli S, Puri R, Verma IC. Nahar R, et al. Among authors: verma ic. Indian J Orthop. 2009 Apr;43(2):194-6. doi: 10.4103/0019-5413.50856. Indian J Orthop. 2009. PMID: 19838370 Free PMC article.
Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNA.
Bashyam MD, Chaudhary AK, Reddy EC, Devi AR, Savithri GR, Ratheesh R, Bashyam L, Mahesh E, Sen D, Puri R, Verma IC, Nampoothiri S, Vaidyanathan S, Chandrashekar MD, Kantheti P. Bashyam MD, et al. Among authors: verma ic. Mol Genet Metab. 2010 May;100(1):96-9. doi: 10.1016/j.ymgme.2010.01.016. Epub 2010 Feb 2. Mol Genet Metab. 2010. PMID: 20188615
415 results