Anwar K - Search Results

1

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

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

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

4

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.

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

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

8

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.

9

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32.

Bessant DA, Anwar K, Khaliq S, Hameed A, Ismail M, Payne AM, Mehdi SQ, Bhattacharya SS. Bessant DA, et al. Among authors: anwar k. Br J Ophthalmol. 1999 Aug;83(8):919-22. doi: 10.1136/bjo.83.8.919. Br J Ophthalmol. 1999. PMID: 10413693 Free PMC article.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

225 results

Search Page

Filters