The role of phospholipases A2 in schizophrenia von Law, M H, Cotton, R G H, Berger, G E

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The use of resolvases T4 endonuclease VII and T7 endonuclease I in mutation detection von BABON, J. J, MCKENZIE, M, COTTON, R. G. H

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Neuropathology of immunohistochemically identified brainstem neurons in Parkinson's disease von Halliday, G. M., Li, Y. W., Blumbergs, P. C., Joh, T. H., Cotton, R. G. H., Howe, P. R. C., Blessing, W. W., Geffen, L. B.

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General mutation databases: analysis and review von George, R A, Smith, T D, Callaghan, S, Hardman, L, Pierides, C, Horaitis, O, Wouters, M A, Cotton, R G H

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Distribution of monoamine-synthesizing neurons in the human medulla oblongata von Halliday, G. M., Li, Y. W., Joh, T. H., Cotton, R. G. H., Howe, P. R. C., Geffen, L. B., Blessing, W. W.

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Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: Proposed guidelines for improving data collection, distribution, and integration von Olivier, M, Petitjean, A, Teague, J, Forbes, S, Dunnick, J.K, den Dunnen, J.T, Langerød, A, Wilkinson, J.M, Vihinen, M, Cotton, R.G.H, Hainaut, P

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Structure and function of the aromatic amino acid hydroxylases von Hufton, S E, Jennings, I G, Cotton, R G

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Quality standards for DNA sequence variation databases to improve clinical management under development in Australia von Bennetts, B., Caramins, M., Hsu, A., Lau, C., Mead, S., Meldrum, C., Smith, T.D., Suthers, G., Taylor, G.R., Cotton, R.G.H., Tyrrell, V.

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Early-onset Alzheimerʼs disease caused by a novel mutation at codon 219 of the presenilin-1 gene von Smith, M J, Gardner, R J. M, Knight, M A, Forrest, S M, Beyreuther, K, Storey, E, McLean, C A, Cotton, R G. H, Cappal, R, Masters, C L

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structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and data... von Cotton, R.G.H, Auerbach, A.D, Brown, A.F, Carrera, P, Christodoulou, J, Claustres, M, Compton, J, Cox, D.W, De Baere, E, den Dunnen, J.T, Greenblatt, M, Fujiwara, M, Hilbert, P, Jani, A, Lehvaslaiho, H, Nebert, D.W, Verma, I, Vihinen, M

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Response to Stenson et al on the review of general mutation databases von George, R A, Smith, T D, Callaghan, S, Hardman, L, Pierides, C, Horaitis, O, Wouters, M A, Cotton, R G H

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The HUGO Mutation Database Initiative von Cotton, R G H, Horaitis, O

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The Human Genome Project and genome variation von Cotton, R. G. H.

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Recommendations for locus-specific databases and their curation von Cotton, R.G.H, Auerbach, A.D, Beckmann, J.S, Blumenfeld, O.O, Brookes, A.J, Brown, A.F, Carrera, P, Cox, D.W, Gottlieb, B, Greenblatt, M.S, Hilbert, P, Lehvaslaiho, H, Liang, P, Marsh, S, Nebert, D.W, Povey, S, Rossetti, S, Scriver, C.R, Summar, M, Tolan, D.R, Verma, I.C, Vihinen, M, den Dunnen, J.T

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A survey of locus-specific database curation von Cotton, Richard G H, Phillips, Kate, Horaitis, Ourania

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Slowly but surely towards better scanning for mutations von Cotton, Richard G.H.

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Cytoarchitecture of serotonin-synthesizing neurons in the pontine tegmentum of the human brain von Baker, K. G., Halliday, G. M., Halasz, P., Hornung, J-P., Geffen, L. B., Cotton, R. G. H., Törk, I.

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Localization of Cofactor Binding Sites with Monoclonal Anti-Idiotype Antibodies: Phenylalanine Hydroxylase von Jennings, I. G., Kemp, B. E., Cotton, R. G. H.

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In vivo disposal of phenylalanine in phenylketonuria: A study of two siblings von Treacy, E., Pitt, J. J., Seller, K., Thompson, G. N., Ramus, S., Cotton, R. G. H.

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Absence of common trifunctional protein mutation in patients with Alpers disease von Yang, Z., Youil, R., Thorburn, D., Chow, C. W., Cotton, R. G. H., Baldwin, G. S.

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