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Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III.
Pasumarthi D, Gupta N, Sheth J, Jain SJMN, Rungsung I, Kabra M, Ranganath P, Aggarwal S, Phadke SR, Girisha KM, Shukla A, Datar C, Verma IC, Puri RD, Bhavsar R, Mistry M, Sankar VH, Gowrishankar K, Agrawal D, Nair M, Danda S, Soni JP, Dalal A. Pasumarthi D, et al. Among authors: verma ic. J Hum Genet. 2020 Nov;65(11):971-984. doi: 10.1038/s10038-020-0797-8. Epub 2020 Jul 10. J Hum Genet. 2020. PMID: 32651481
Diastrophic dysplasia: a case report.
Mehta L, Verma IC, Soni JP, Singhania RU. Mehta L, et al. Among authors: verma ic. Indian J Pediatr. 1992 Nov-Dec;59(6):755-7. doi: 10.1007/BF02859416. Indian J Pediatr. 1992. PMID: 1340866 No abstract available.
Cytogenetic studies in Down syndrome.
Verma IC, Mathew S, Elango R, Shukla A. Verma IC, et al. Indian Pediatr. 1991 Sep;28(9):991-6. Indian Pediatr. 1991. PMID: 1839389 Review.
Group B meningococcal meningitis in India.
Suri M, Kabra M, Singh S, Rattan A, Verma IC. Suri M, et al. Among authors: verma ic. Scand J Infect Dis. 1994;26(6):771-3. doi: 10.3109/00365549409008652. Scand J Infect Dis. 1994. PMID: 7747107
Phenotype of 49,XXYYY.
Das GP, Shukla A, Verma IC. Das GP, et al. Among authors: verma ic. Clin Genet. 1993 Apr;43(4):196-9. doi: 10.1111/j.1399-0004.1993.tb04447.x. Clin Genet. 1993. PMID: 8330452
A clinical and cytogenetic study of Turner syndrome.
Suri M, Kabra M, Jain U, Sanders V, Saxena R, Shukla A, Singh GV, Verma IC. Suri M, et al. Among authors: verma ic. Indian Pediatr. 1995 Apr;32(4):433-42. Indian Pediatr. 1995. PMID: 8635807
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.
413 results