Kannabiran C - Search Results

1

Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India.

Sultana A, Sridhar MS, Jagannathan A, Balasubramanian D, Kannabiran C, Klintworth GK. Sultana A, et al. Among authors: kannabiran c. Mol Vis. 2003 Dec 22;9:730-4. Mol Vis. 2003. PMID: 14735064 Free article.

2

Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin gene.

Kannabiran C, Rogan PK, Olmos L, Basti S, Rao GN, Kaiser-Kupfer M, Hejtmancik JF. Kannabiran C, et al. Mol Vis. 1998 Oct 23;4:21. Mol Vis. 1998. PMID: 9788845 Free article.

3

Molecular genetics of cataract.

Kannabiran C, Balasubramanian D. Kannabiran C, et al. Indian J Ophthalmol. 2000 Mar;48(1):5-13. Indian J Ophthalmol. 2000. PMID: 11271936 Free article. Review.

4

Mutational analysis of the RB1 gene in Indian patients with retinoblastoma.

Ata-ur-Rasheed M, Vemuganti Gk, Honavar Sg, Ahmed N, Hasnain Se, Kannabiran C. Ata-ur-Rasheed M, et al. Among authors: kannabiran c. Ophthalmic Genet. 2002 Jun;23(2):121-8. doi: 10.1076/opge.23.2.121.2211. Ophthalmic Genet. 2002. PMID: 12187430

5

Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations.

Kiran VS, Kannabiran C, Chakravarthi K, Vemuganti GK, Honavar SG. Kiran VS, et al. Among authors: kannabiran c. Hum Mutat. 2003 Oct;22(4):339. doi: 10.1002/humu.9181. Hum Mutat. 2003. PMID: 12955724

6

TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.

Chakravarthi SV, Kannabiran C, Sridhar MS, Vemuganti GK. Chakravarthi SV, et al. Among authors: kannabiran c. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):121-5. doi: 10.1167/iovs.04-0440. Invest Ophthalmol Vis Sci. 2005. PMID: 15623763

7

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.

Kannabiran C, Sridhar MS, Chakravarthi SK, Vemuganti GK, Lakshmipathi M. Kannabiran C, et al. Arch Ophthalmol. 2005 Aug;123(8):1127-33. doi: 10.1001/archopht.123.8.1127. Arch Ophthalmol. 2005. PMID: 16087849

8

Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy.

Sultana A, Sridhar MS, Klintworth GK, Balasubramanian D, Kannabiran C. Sultana A, et al. Among authors: kannabiran c. Clin Genet. 2005 Nov;68(5):454-60. doi: 10.1111/j.1399-0004.2005.00517.x. Clin Genet. 2005. PMID: 16207214

9

Homozygous null mutations in the ABCA4 gene in two families with autosomal recessive retinal dystrophy.

Singh HP, Jalali S, Hejtmancik JF, Kannabiran C. Singh HP, et al. Among authors: kannabiran c. Am J Ophthalmol. 2006 May;141(5):906-13. doi: 10.1016/j.ajo.2005.12.009. Epub 2006 Mar 20. Am J Ophthalmol. 2006. PMID: 16546111

10

TGFBI gene mutations in corneal dystrophies.

Kannabiran C, Klintworth GK. Kannabiran C, et al. Hum Mutat. 2006 Jul;27(7):615-25. doi: 10.1002/humu.20334. Hum Mutat. 2006. PMID: 16683255 Review.

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