Mathew CG - Search Results

1

Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.

Prescott NJ, Dominy KM, Kubo M, Lewis CM, Fisher SA, Redon R, Huang N, Stranger BE, Blaszczyk K, Hudspith B, Parkes G, Hosono N, Yamazaki K, Onnie CM, Forbes A, Dermitzakis ET, Nakamura Y, Mansfield JC, Sanderson J, Hurles ME, Roberts RG, Mathew CG. Prescott NJ, et al. Among authors: mathew cg. Hum Mol Genet. 2010 May 1;19(9):1828-39. doi: 10.1093/hmg/ddq041. Epub 2010 Jan 27. Hum Mol Genet. 2010. PMID: 20106866 Free PMC article.

2

A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.

Differ AM, Bobrow M, Mathew CG. Differ AM, et al. Among authors: mathew cg. Hum Genet. 1992 Aug;89(6):689. doi: 10.1007/BF00221966. Hum Genet. 1992. PMID: 1355071

3

A MseI polymorphism in exon 48 of the dystrophin gene.

Yau SC, Roberts RG, Bentley DR, Mathew CG, Bobrow M. Yau SC, et al. Among authors: mathew cg. Nucleic Acids Res. 1991 Oct 25;19(20):5803. doi: 10.1093/nar/19.20.5803-a. Nucleic Acids Res. 1991. PMID: 1682892 Free PMC article.

4

Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.

Abbs S, Roberts RG, Mathew CG, Bentley DR, Bobrow M. Abbs S, et al. Among authors: mathew cg. Genomics. 1990 Aug;7(4):602-6. doi: 10.1016/0888-7543(90)90205-9. Genomics. 1990. PMID: 1974880

5

A nonsense mutation and exon skipping in the Fanconi anaemia group C gene.

Gibson RA, Hajianpour A, Murer-Orlando M, Buchwald M, Mathew CG. Gibson RA, et al. Among authors: mathew cg. Hum Mol Genet. 1993 Jun;2(6):797-9. doi: 10.1093/hmg/2.6.797. Hum Mol Genet. 1993. PMID: 7689011

6

EcoRI RFLP in the Fanconi anaemia complementation group C gene (FACC).

Gibson RA, Savoia A, Buchwald M, Mathew CG. Gibson RA, et al. Among authors: mathew cg. Hum Mol Genet. 1993 Sep;2(9):1509. doi: 10.1093/hmg/2.9.1509-a. Hum Mol Genet. 1993. PMID: 7902167 No abstract available.

7

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.

Yau SC, Roberts RG, Bobrow M, Mathew CG. Yau SC, et al. Among authors: mathew cg. Lancet. 1993 Jan 30;341(8840):273-5. doi: 10.1016/0140-6736(93)92618-4. Lancet. 1993. PMID: 8093919

8

Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR.

Gibson RA, Buchwald M, Roberts RG, Mathew CG. Gibson RA, et al. Among authors: mathew cg. Hum Mol Genet. 1993 Jan;2(1):35-8. doi: 10.1093/hmg/2.1.35. Hum Mol Genet. 1993. PMID: 8490620

9

Analysis of the contribution of HLA genes to genetic predisposition in inflammatory bowel disease.

Naom I, Lee J, Ford D, Bowman SJ, Lanchbury JS, Haris I, Hodgson SV, Easton D, Lennard-Jones J, Mathew CG. Naom I, et al. Among authors: mathew cg. Am J Hum Genet. 1996 Jul;59(1):226-33. Am J Hum Genet. 1996. PMID: 8659528 Free PMC article.

10

Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitis.

Mirza MM, Lee J, Teare D, Hugot JP, Laurent-Puig P, Colombel JF, Hodgson SV, Thomas G, Easton DF, Lennard-Jones JE, Mathew CG. Mirza MM, et al. Among authors: mathew cg. J Med Genet. 1998 Mar;35(3):218-21. doi: 10.1136/jmg.35.3.218. J Med Genet. 1998. PMID: 9541106 Free PMC article.

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