Author/Creator: Mathew, C G - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Mathew, C G

1. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods. Issue 5 (May 1991)

Authors:: Abbs, S; Yau, S C; Clark, S; Mathew, C G; Bobrow, M
Journal:: Journal of medical genetics
Issue:: Volume 28:Issue 5(1991)
Page Start:: 304
Record Type:: Journal Article
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2. A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype. Issue 1 (January 1993)

Authors:: Milner, R D; Khallouf, K A; Gibson, R; Hajianpour, A; Mathew, C G
Journal:: Archives of disease in childhood
Issue:: Volume 68:Issue 1(1993)
Page Start:: 101
Record Type:: Journal Article
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3. A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci. Issue 3 (March 1995)

Authors:: Wang, Q; Green, E; Bobrow, M; Mathew, C G
Journal:: Journal of medical genetics
Issue:: Volume 32:Issue 3(1995)
Page Start:: 170
Record Type:: Journal Article
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4. A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255. Issue 9 (September 1995)

Authors:: Bennett, C P; Barnicoat, A J; Cotter, F; Wang, Q; Mathew, C G
Journal:: Journal of medical genetics
Issue:: Volume 32:Issue 9(1995)
Page Start:: 757
Record Type:: Journal Article
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5. Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. Issue 7 (July 1996)

Authors:: Yau, S C; Bobrow, M; Mathew, C G; Abbs, S J
Journal:: Journal of medical genetics
Issue:: Volume 33:Issue 7(1996)
Page Start:: 550
Record Type:: Journal Article
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6. Clinical, cytogenetic, and molecular analysis of three families with FRAXE. Issue 1 (January 1997)

Authors:: Barnicoat, A J; Wang, Q; Turk, J; Green, E; Mathew, C G; Flynn, G; Buckle, V; Hirst, M; Davies, K; Bobrow, M
Journal:: Journal of medical genetics
Issue:: Volume 34:Issue 1(1997)
Page Start:: 13
Record Type:: Journal Article
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7. Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn disease. Issue 11 (27th July 2007)

Authors:: Lewis, C M; Whitwell, S C L; Forbes, A; Sanderson, J; Mathew, C G; Marteau, T M
Journal:: Journal of medical genetics
Issue:: Volume 44:Issue 11(2007)
Page Start:: 689
Record Type:: Journal Article
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8. Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitis. Issue 3 (March 1998)

Authors:: Mirza, M M; Lee, J; Teare, D; Hugot, J P; Laurent-Puig, P; Colombel, J F; Hodgson, S V; Thomas, G; Easton, D F; Lennard-Jones, J E; Mathew, C G
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 3(1998)
Page Start:: 218
Record Type:: Journal Article
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9. Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease. Issue 2 (1st February 2001)

Authors:: Hampe, J; Lynch, N J; Daniels, S; Bridger, S; Macpherson, A J S; Stokkers, P; Forbes, A; Lennard-Jones, J E; Mathew, C G; Curran, M E; Schreiber, S
Journal:: Gut
Issue:: Volume 48:Issue 2(2001)
Page Start:: 191
Record Type:: Journal Article
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10. Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?. Issue 9 (11th August 2004)

Authors:: Cuthbert, A P; Fisher, S A; Lewis, C M; Mathew, C G; Sanderson, J; Forbes, A
Journal:: Gut
Issue:: Volume 53:Issue 9(2004)
Page Start:: 1386
Record Type:: Journal Article
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