Verma IC - Search Results

1

KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1.

Vyas B, Puri RD, Namboodiri N, Nair M, Sharma D, Movva S, Saxena R, Bohora S, Aggarwal N, Vora A, Kumar J, Singh T, Verma IC. Vyas B, et al. Among authors: verma ic. Am J Med Genet A. 2016 Jun;170(6):1510-9. doi: 10.1002/ajmg.a.37636. Epub 2016 Apr 4. Am J Med Genet A. 2016. PMID: 27041150 Review.

2

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.

3

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

4

Regional distribution of beta-thalassemia mutations in India.

Verma IC, Saxena R, Thomas E, Jain PK. Verma IC, et al. Hum Genet. 1997 Jul;100(1):109-13. doi: 10.1007/s004390050475. Hum Genet. 1997. PMID: 9225979

5

Detection of beta-thalassaemia mutation insertion ATCT at codon 47/48 by ARMS technique for screening & prenatal diagnosis.

Saxena R, Thomas E, Verma IC. Saxena R, et al. Among authors: verma ic. Indian J Med Res. 1997 Jun;105:275-7. Indian J Med Res. 1997. PMID: 9277041

6

Prenatal diagnosis of beta-thalassaemia: experience in a developing country.

Saxena R, Jain PK, Thomas E, Verma IC. Saxena R, et al. Among authors: verma ic. Prenat Diagn. 1998 Jan;18(1):1-7. Prenat Diagn. 1998. PMID: 9483634

7

A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACT CCT GAG-> ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing.

Saxena R, Moi L, Demurtas M, Rosatelli MC, Cao A, Verma IC. Saxena R, et al. Among authors: verma ic. Indian J Med Res. 2000 Jan;111:24-7. Indian J Med Res. 2000. PMID: 10793490

8

Congenital myotonic dystrophy.

Gulati S, Kabra M, Gera S, Kalra V, Saxena R, Verma IC. Gulati S, et al. Among authors: verma ic. Indian J Pediatr. 2001 May;68(5):451-3. doi: 10.1007/BF02723026. Indian J Pediatr. 2001. PMID: 11407162

9

Genetic counseling and prenatal diagnosis in India--experience at Sir Ganga Ram Hospital.

Verma IC, Saxena R, Lall M, Bijarnia S, Sharma R. Verma IC, et al. Indian J Pediatr. 2003 Apr;70(4):293-7. doi: 10.1007/BF02723582. Indian J Pediatr. 2003. PMID: 12793304

10

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

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