Khaliq S - 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. Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3709-12. Invest Ophthalmol Vis Sci. 2000. PMID: 11053266

2

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: khaliq s. Am J Hum Genet. 1998 May;62(5):1113-6. doi: 10.1086/301843. Am J Hum Genet. 1998. PMID: 9545413 Free PMC article.

3

Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online.

Bessant DA, Khaliq S, Hameed A, Anwar K, Payne AM, Mehdi SQ, Bhattacharya SS. Bessant DA, et al. Among authors: khaliq s. Hum Mutat. 1999;13(1):83. doi: 10.1002/(SICI)1098-1004(1999)13:1<83::AID-HUMU12>3.0.CO;2-5. Hum Mutat. 1999. PMID: 10189219

4

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: khaliq s. 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.

5

Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.

Khaliq S, Hameed A, Ismail M, Mehdi SQ, Bessant DA, Payne AM, Bhattacharya SS. Khaliq S, et al. Am J Hum Genet. 1999 Aug;65(2):571-4. doi: 10.1086/302493. Am J Hum Genet. 1999. PMID: 10417302 Free PMC article. No abstract available.

6

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.

Berry V, Mackay D, Khaliq S, Francis PJ, Hameed A, Anwar K, Mehdi SQ, Newbold RJ, Ionides A, Shiels A, Moore T, Bhattacharya SS. Berry V, et al. Among authors: khaliq s. Hum Genet. 1999 Jul-Aug;105(1-2):168-70. doi: 10.1007/s004399900094. Hum Genet. 1999. PMID: 10480374

7

African and Levantine origins of Pakistani YAP+ Y chromosomes.

Qamar R, Ayub Q, Khaliq S, Mansoor A, Karafet T, Mehdi SQ, Hammer MF. Qamar R, et al. Among authors: khaliq s. Hum Biol. 1999 Oct;71(5):745-55. Hum Biol. 1999. PMID: 10510568

8

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. Sohocki MM, et al. Among authors: khaliq s. Nat Genet. 2000 Jan;24(1):79-83. doi: 10.1038/71732. Nat Genet. 2000. PMID: 10615133 Free PMC article.

9

HLA polymorphisms in ethnic groups from Pakistan.

Mohyuddin A, Ayub Q, Qamar R, Khaliq S, Mansoor A, Mehdi SQ. Mohyuddin A, et al. Among authors: khaliq s. Transplant Proc. 1999 Dec;31(8):3350-1. doi: 10.1016/s0041-1345(99)00821-0. Transplant Proc. 1999. PMID: 10616502 No abstract available.

10

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: khaliq s. Invest Ophthalmol Vis Sci. 2000 Mar;41(3):629-33. Invest Ophthalmol Vis Sci. 2000. PMID: 10711674 Free article.

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