Kumar A - Search Results

1

Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma.

Markandaya M, Ramesh TK, Selvaraju V, Dorairaj SK, Prakash R, Shetty J, Kumar A. Markandaya M, et al. Among authors: kumar a. Ophthalmic Genet. 2004 Mar;25(1):11-23. doi: 10.1076/opge.25.1.11.28995. Ophthalmic Genet. 2004. PMID: 15255110

2

Clinical phenotype and linkage analysis of the congenital fibrosis of the extraocular muscles in an Indian family.

Venkatesh CP, Pillai VS, Raghunath A, Prakash VS, Vathsala R, Pericak-Vance MA, Kumar A. Venkatesh CP, et al. Among authors: kumar a. Mol Vis. 2002 Aug 14;8:294-7. Mol Vis. 2002. PMID: 12181522 Free article.

3

Primary microcephaly: microcephalin and ASPM determine the size of the human brain.

Kumar A, Markandaya M, Girimaji SC. Kumar A, et al. J Biosci. 2002 Dec;27(7):629-32. doi: 10.1007/BF02708369. J Biosci. 2002. PMID: 12571366 No abstract available.

4

Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome.

Selvaraju V, Markandaya M, Prasad PV, Sathyan P, Sethuraman G, Srivastava SC, Thakker N, Kumar A. Selvaraju V, et al. Among authors: kumar a. BMC Med Genet. 2003 Jul 12;4:5. doi: 10.1186/1471-2350-4-5. BMC Med Genet. 2003. PMID: 12857359 Free PMC article.

5

Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5.

Bajaj V, Markandaya M, Krishna L, Kumar A. Bajaj V, et al. Among authors: kumar a. BMC Genet. 2004 Jun 3;5:13. doi: 10.1186/1471-2156-5-13. BMC Genet. 2004. PMID: 15175115 Free PMC article.

6

Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.

Kumar A, Shetty J, Kumar B, Blanton SH. Kumar A, et al. Among authors: kumar b. Mol Vis. 2004 Jun 15;10:399-402. Mol Vis. 2004. PMID: 15215745 Free article.

7

Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C).

Kumar A, Babu M, Raghunath A, Venkatesh CP. Kumar A, et al. Mol Vis. 2004 Jul 9;10:445-9. Mol Vis. 2004. PMID: 15257268 Free article.

8

Genetic analysis of primary microcephaly in Indian families: novel ASPM mutations.

Kumar A, Blanton SH, Babu M, Markandaya M, Girimaji SC. Kumar A, et al. Clin Genet. 2004 Oct;66(4):341-8. doi: 10.1111/j.1399-0004.2004.00304.x. Clin Genet. 2004. PMID: 15355437

9

Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.

Kumar A, Babu M, Kimberling WJ, Venkatesh CP. Kumar A, et al. Mol Vis. 2004 Nov 24;10:910-6. Mol Vis. 2004. PMID: 15592175 Free article.

10

Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations.

Ali M, Venkatesh C, Ragunath A, Kumar A. Ali M, et al. Among authors: kumar a. Ophthalmic Genet. 2004 Dec;25(4):247-55. doi: 10.1080/13816810490498198. Ophthalmic Genet. 2004. PMID: 15621877

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