Ismail M - Search Results

1

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: ismail m. 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.

2

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: ismail m. Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1436-8. Invest Ophthalmol Vis Sci. 2001. PMID: 11381043 Free article.

3

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: ismail m. Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2225-8. Invest Ophthalmol Vis Sci. 2001. PMID: 11527934

4

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. Among authors: ismail m. 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.

5

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

6

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

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: ismail m. Arch Ophthalmol. 2004 Jul;122(7):1029-37. doi: 10.1001/archopht.122.7.1029. Arch Ophthalmol. 2004. PMID: 15249368

8

Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy.

Hameed A, Abid A, Aziz A, Ismail M, Mehdi SQ, Khaliq S. Hameed A, et al. Among authors: ismail m. J Med Genet. 2003 Aug;40(8):616-9. doi: 10.1136/jmg.40.8.616. J Med Genet. 2003. PMID: 12920076 Free PMC article. No abstract available.

9

Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa.

Khaliq S, Abid A, Ismail M, Hameed A, Mohyuddin A, Lall P, Aziz A, Anwar K, Mehdi SQ. Khaliq S, et al. Among authors: ismail m. J Med Genet. 2005 May;42(5):436-8. doi: 10.1136/jmg.2004.024281. J Med Genet. 2005. PMID: 15863674 Free PMC article. No abstract available.

10

Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases.

Abid A, Ismail M, Mehdi SQ, Khaliq S. Abid A, et al. Among authors: ismail m. J Med Genet. 2006 Apr;43(4):378-81. doi: 10.1136/jmg.2005.035055. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199541 Free PMC article.

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