WS17.1 The ancient origin of F508del-CF: When and where the mutation arose von Farrell, P.M, Génin, E, Férec, C, Giteau, K, Frischer, T, Renner, S, Riss, K, Barton, D.E, Repetto, T, Tzetis, M, Macek, M, Dunø, M, Rogers, M, Sahbatou, M, Rouault, K, Fichou, Y, Le Maréchal, C

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WS3.1 Changing incidence of CF in Ireland? von Mayne, P, Roche, G, Greenwood, C, Cooney, D, Rogers, M, Roring, S, McDevitt, T, Barton, D.E

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Genotypes and borderline sweat tests in Irish CF patients -an update von King, C.M, Rogers, M, McDevitt, T, Lambert, D, Barton, D.E, Lynch, S.A

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Reply to Sajantila and Budowle von Barton, D.E, Claustres, M, Kozich, V, Dequeker, Els, Fowler, B, Hehir-Kwa, J.Y, Miller, K, Oosterwijk, C, Peterlin, B, van Ravenswaaij-Arts, C, Zimmerman, U, Zuffardi, O, Hastings, R.J

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The detection of large deletions or duplications in genomic DNA von Armour, J.A.L., Barton, D.E., Cockburn, D.J., Taylor, G.R.

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Rapid-onset dystonia-parkinsonism : A clinical and genetic analysis of a new kindred von PITTOCK, S. J, JOYCE, C, O'KEANE, V, HUGLE, B, HARDIMAN, O, BRETT, F, GREEN, A. J, BARTON, D. E, KING, M. D, WEBB, D. W

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A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in ur... von Darlow, J. M., Dobson, M. G., Darlay, R., Molony, C. M., Hunziker, M., Green, A. J., Cordell, H. J., Puri, P., Barton, D. E.

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Predictive testing for BRCA1 and 2 mutations: a male contribution von Daly, P. A., Nolan, C., Green, A., Ormiston, W., Cody, N., McDevitt, T., O’hIci, B., Byrne, D., McDermott, E., Carney, D. N., O’Higgins, N., Barton, D. E.

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The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility von QUINTANA-MURCI, L, KRAUSZ, C, LEE, A. C, JOBLING, M. A, MCELREAVEY, K, HEYER, E, GROMOLL, J, SEIFER, I, BARTON, D. E, BARRETT, T, SKAKKEBAEK, N. E, RAJPERT-DE MEYTS, E, MITCHELL, M

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Identification of a cDNA Encoding a Parathyroid Hormone-Like Peptide from a Human Tumor Associated with Humoral Hypercalcemia of Malignancy von Mangin, Marguerite, Webb, Andrew C., Dreyer, Barbara E., Posillico, James T., Ikeda, Kyoji, Weir, Eleanor C., Stewart, Andrew F., Bander, Neil H., Milstone, Leonard, Barton, David E., Francke, Uta, Broadus, Arthur E.

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Typical Friedreich's ataxia without GAA expansions and GAA expansions without typical Friedreich's ataxia von MCCABE, D. J. H, RYAN, F, MOORE, D. P, MCQUAID, S, KING, M. D, KELLY, A, DALY, K, BARTON, D. E, MURPHY, R. P

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Genetic Services in Ireland von Barton, D.E.

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Mapping of genes for inhibin subunits α, βA, and βB on human and mouse chromosomes and studies of jsd mice von Barton, D.E., Yang-Feng, T.L., Mason, A.J., Seeburg, P.H., Francke, U.

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Pyrolysis studies with Jojaba oil von Landis, P.S, Craver, R.H.Sr, Barton, D.E

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Molecular analysis of the Mov 34 mutation: transcript disrupted by proviral integration in mice is conserved in Drosophila von Gridley, T, Gray, D A, Orr-Weaver, T, Soriano, P, Barton, D E, Francke, U, Jaenisch, R

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Issues in Huntington's disease testing von RUBINSZTEIN, D.C., BARTON, D.E., FERGUSON-SMITH, M.A.

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Genetic Mapping of X-Linked Ocular Albinism: Linkage Analysis in a Large Newfoundland Kindred von Charles, Stephen J., Green, Jane S., Moore, Anthony T., Barton, David E., Yates, John R.W.

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Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patients von Rubinsztein, David C., Leggo, Jayne, Goodburn, Sandy, Barton, David E., Ferguson-Smith, Malcolm A.

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Level of expression and chromosome mapping of the mouse cholecystokinin gene: Implications for murine models of genetic obesity von Friedman, J.M., Schneider, B.S., Barton, D.E., Francke, U.

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Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: Functional locus identified by its amplification in hydroxyurea-resista... von Yang-Feng, T.L., Barton, D.E., Thelander, L., Lewis, W.H., Srinivasan, P.R., Francke, U.

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