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A genetic journey through cancer: from rarity and family to aspirin and nanowires by Burn J
Published 2012-04-01
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Bowel cancer chemoprevention - ready for the clinic? by Burn J
Published 2012-04-01
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Acknowledgment to the Reviewers of <i>Eur. Burn J.</i> in 2022 by Eur. Burn J. Editorial Office
Published 2023-01-01
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PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28. by Lindsay, S, Splitt, M, Edney, S, Berney, T, Knight, S, Davies, K, O'Brien, O, Gale, M, Burn, J
Published 1996Journal article -
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Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134). by Wadey, R, Daw, S, Wickremasinghe, A, Roberts, C, Wilson, D, Goodship, J, Burn, J, Halford, S, Scambler, P
Published 1993Journal article -
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Aspirin, salicylates and cancer by Morgan, G, Rothwell, P, Burn, J, Chan, A, Mur, L, Morton, D, Cuzick, J, McVie, G
Published 2011Journal article -
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Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia. by Bilous, R, Murty, G, Parkinson, D, Thakker, R, Coulthard, MG, Burn, J, Mathias, D, Kendall-Taylor, P
Published 1992Journal article -
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Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. by Carey, A, Kelly, D, Halford, S, Wadey, R, Wilson, D, Goodship, J, Burn, J, Paul, T, Sharkey, A, Dumanski, J
Published 1992Journal article -
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Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X). by Gibbons, R, Brueton, L, Buckle, V, Burn, J, Clayton-Smith, J, Davison, B, Gardner, R, Homfray, T, Kearney, L, Kingston, H
Published 1995Journal article -
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Aspirin and non-steroidal anti-inflammatory drugs for cancer prevention: an international consensus statement. by Cuzick, J, Otto, F, Baron, J, Brown, P, Burn, J, Greenwald, P, Jankowski, J, La Vecchia, C, Meyskens, F, Senn, H, Thun, M
Published 2009Journal article -
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MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES by Scambler, P, Halford, S, Wadey, R, Lindsay, E, Kelly, D, Wilson, D, Goodship, J, Burn, J, Goldberg, R, Shprintzen, R, Williamson, R, Carey, A
Published 1991Journal article -
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Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. by Douglas, J, Cilliers, D, Coleman, K, Tatton-Brown, K, Barker, K, Bernhard, B, Burn, J, Huson, S, Josifova, D, Lacombe, D, Malik, M, Mansour, S, Reid, E, Cormier-Daire, V, Cole, T, Rahman, N
Published 2007Journal article -
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CATCH-22 - CAN MOLECULAR GENETICS EXPLAIN THE PHENOTYPE by Halford, S, Wadey, R, Roberts, C, Daw, S, Whiting, J, Odonnell, H, Dunham, I, Bentley, D, Lindsay, E, Baldini, A, Francis, F, Lehrach, H, Williamson, R, Wilson, D, Goodship, J, Cross, I, Burn, J, Scambler, P
Published 1995Conference item -
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MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer. by Hitchins, M, Williams, R, Cheong, K, Halani, N, Lin, V, Packham, D, Ku, S, Buckle, A, Hawkins, N, Burn, J, Gallinger, S, Goldblatt, J, Kirk, J, Tomlinson, I, Scott, R, Spigelman, A, Suter, C, Martin, D, Suthers, G, Ward, R
Published 2005Journal article -
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Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes. by Toutain, A, Dessay, B, Ronce, N, Ferrante, M, Tranchemontagne, J, Newbury-Ecob, R, Wallgren-Pettersson, C, Burn, J, Kaplan, J, Rossi, A, Russo, S, Walpole, I, Hartsfield, J, Oyen, N, Nemeth, A, Bitoun, P, Trump, D, Moraine, C, Franco, B
Published 2002Journal article -
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Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. by Griffin, H, Hall, D, Topf, A, Eden, J, Stuart, A, Parsons, J, Peart, I, Deanfield, J, O'Sullivan, J, Babu-Narayan, S, Gatzoulis, M, Bu'lock, F, Bhattacharya, S, Bentham, J, Farrall, M, Granados Riveron, J, Brook, J, Burn, J, Cordell, H, Goodship, J, Keavney, B
Published 2009Journal article