Anwar K - Search Results

1

A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.

Hameed A, Khaliq S, Ismail M, Anwar K, Ebenezer ND, Jordan T, Mehdi SQ, Payne AM, Bhattacharya SS. Hameed A, et al. Among authors: anwar k. Invest Ophthalmol Vis Sci. 2000 Mar;41(3):629-33. Invest Ophthalmol Vis Sci. 2000. PMID: 10711674 Free article.

2

A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.

Khaliq S, Hameed A, Ismail M, Anwar K, Mehdi SQ. Khaliq S, et al. Among authors: anwar k. Invest Ophthalmol Vis Sci. 2002 Jul;43(7):2083-7. Invest Ophthalmol Vis Sci. 2002. PMID: 12091400

3

Mutation screening of Pakistani families with congenital eye disorders.

Khaliq S, Abid A, Hameed A, Anwar K, Mohyuddin A, Azmat Z, Shami SA, Ismail M, Mehdi SQ. Khaliq S, et al. Among authors: anwar k. Exp Eye Res. 2003 Mar;76(3):343-8. doi: 10.1016/s0014-4835(02)00304-4. Exp Eye Res. 2003. PMID: 12573663

4

Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy BP, Mehdi SQ, Payne AM, Bhattacharya SS. Khaliq S, et al. Among authors: anwar k. Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3709-12. Invest Ophthalmol Vis Sci. 2000. PMID: 11053266

5

A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.

Hameed A, Khaliq S, Ismail M, Anwar K, Mehdi SQ, Bessant D, Payne AM, Bhattacharya SS. Hameed A, et al. Among authors: anwar k. Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1436-8. Invest Ophthalmol Vis Sci. 2001. PMID: 11381043 Free article.

6

Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy B, Payne AM, Bhattacharya SS, Mehdi SQ. Khaliq S, et al. Among authors: anwar k. Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2225-8. Invest Ophthalmol Vis Sci. 2001. PMID: 11527934

7

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.

Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, Bhattacharya SS, Bird AC, Kaplan J, Maumenee IH. Dharmaraj S, et al. Among authors: anwar k. Arch Ophthalmol. 2004 Jul;122(7):1029-37. doi: 10.1001/archopht.122.7.1029. Arch Ophthalmol. 2004. PMID: 15249368

8

Gene symbol: AIPL1. Disease: LCA4.

Khaliq S, Abid A, Hameed A, Anwar K, Mohyuddin A, Ismail M, Mehdi SQ. Khaliq S, et al. Among authors: anwar k. Hum Genet. 2005 May;116(6):542. Hum Genet. 2005. PMID: 15991325 No abstract available.

9

Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes.

Ismail M, Abid A, Anwar K, Qasim Mehdi S, Khaliq S. Ismail M, et al. Among authors: anwar k. J Hum Genet. 2006;51(9):827-831. doi: 10.1007/s10038-006-0028-y. Epub 2006 Aug 3. J Hum Genet. 2006. PMID: 16897189

10

A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.

Bessant DA, Khaliq S, Hameed A, Anwar K, Mehdi SQ, Payne AM, Bhattacharya SS. Bessant DA, et al. Among authors: anwar k. Am J Hum Genet. 1998 May;62(5):1113-6. doi: 10.1086/301843. Am J Hum Genet. 1998. PMID: 9545413 Free PMC article.

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