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Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing.
Bijarnia-Mahay S, Häberle J, Jalan AB, Puri RD, Kohli S, Kudalkar K, Rüfenacht V, Gupta D, Maurya D, Verma J, Shigematsu Y, Yamaguchi S, Saxena R, Verma IC. Bijarnia-Mahay S, et al. Among authors: verma j, verma ic. Orphanet J Rare Dis. 2018 Oct 1;13(1):174. doi: 10.1186/s13023-018-0908-1. Orphanet J Rare Dis. 2018. PMID: 30285816 Free PMC article.
The tricho-rhino-phalangeal syndromes I and II.
Mehta L, Jain PK, Saxena R, Verma IC. Mehta L, et al. Among authors: verma ic. Indian J Pediatr. 1992 May-Jun;59(3):373-7. doi: 10.1007/BF02821808. Indian J Pediatr. 1992. PMID: 1398874 No abstract available.
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
Burden of genetic disorders in India.
Verma IC. Verma IC. Indian J Pediatr. 2000 Dec;67(12):893-8. doi: 10.1007/BF02723953. Indian J Pediatr. 2000. PMID: 11262988
415 results