Anwar R - Search Results

1

Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.

Hewitt AW, Bennett SL, Richards JE, Dimasi DP, Booth AP, Inglehearn C, Anwar R, Yamamoto T, Fingert JH, Héon E, Craig JE, Mackey DA. Hewitt AW, et al. Among authors: anwar r. Arch Ophthalmol. 2007 Jan;125(1):98-104. doi: 10.1001/archopht.125.1.98. Arch Ophthalmol. 2007. PMID: 17210859

2

Genetic screening in a large family with juvenile onset primary open angle glaucoma.

Booth AP, Anwar R, Chen H, Churchill AJ, Jay J, Polansky J, Nguyen T, Markham AF. Booth AP, et al. Among authors: anwar r. Br J Ophthalmol. 2000 Jul;84(7):722-6. doi: 10.1136/bjo.84.7.722. Br J Ophthalmol. 2000. PMID: 10873982 Free PMC article.

3

The genetics of primary open angle glaucoma.

Booth A, Churchill A, Anwar R, Menage M, Markham A. Booth A, et al. Among authors: anwar r. Br J Ophthalmol. 1997 May;81(5):409-14. doi: 10.1136/bjo.81.5.409. Br J Ophthalmol. 1997. PMID: 9227209 Free PMC article. Review. No abstract available.

4

Novel primer specific false terminations during DNA sequencing reactions: danger of inaccuracy of mutation analysis in molecular diagnostics.

Anwar R, Booth A, Churchill AJ, Markham AF. Anwar R, et al. Clin Mol Pathol. 1996 Oct;49(5):M312-4. doi: 10.1136/mp.49.5.m312. Clin Mol Pathol. 1996. PMID: 16696096 Free PMC article.

5

PAX 6 is normal in most cases of Peters' anomaly.

Churchill AJ, Booth AP, Anwar R, Markham AF. Churchill AJ, et al. Among authors: anwar r. Eye (Lond). 1998;12 ( Pt 2):299-303. doi: 10.1038/eye.1998.69. Eye (Lond). 1998. PMID: 9683959

6

Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype.

Carr IM, Diggle CP, Khan K, Inglehearn C, McKibbin M, Bonthron DT, Markham AF, Anwar R, Dobbie A, Pena SD, Ali M. Carr IM, et al. Among authors: anwar r. PLoS One. 2012;7(8):e43466. doi: 10.1371/journal.pone.0043466. Epub 2012 Aug 17. PLoS One. 2012. PMID: 22912880 Free PMC article.

7

Amplification refractory mutation system for prenatal diagnosis and carrier assessment in cystic fibrosis.

Newton CR, Heptinstall LE, Summers C, Super M, Schwarz M, Anwar R, Graham A, Smith JC, Markham AF. Newton CR, et al. Among authors: anwar r. Lancet. 1989 Dec 23-30;2(8678-8679):1481-3. doi: 10.1016/s0140-6736(89)92931-0. Lancet. 1989. PMID: 2574768

8

Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population.

Smith JC, Anwar R, Riley J, Jenner D, Markham AF, Jeffreys AJ. Smith JC, et al. Among authors: anwar r. J Forensic Sci Soc. 1990 Jan-Feb;30(1):19-32. doi: 10.1016/s0015-7368(90)73298-7. J Forensic Sci Soc. 1990. PMID: 2319227

9

Factor XIII deficiency.

Anwar R, Miloszewski KJ. Anwar R, et al. Br J Haematol. 1999 Dec;107(3):468-84. doi: 10.1046/j.1365-2141.1999.01648.x. Br J Haematol. 1999. PMID: 10583246 Free article. Review. No abstract available.

10

Identification of autosomal recessive disease loci using out-bred nuclear families.

Carr IM, Diggle CP, Touqan N, Anwar R, Sheridan EG, Bonthron DT, Johnson CA, Ali M, Markham AF. Carr IM, et al. Among authors: anwar r. Hum Mutat. 2012 Feb;33(2):338-42. doi: 10.1002/humu.21645. Epub 2011 Nov 28. Hum Mutat. 2012. PMID: 22052625

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