Allelic and Locus Heterogeneity in Inherited Venous Malformations von Calvert, Jennifer T., Riney, Travis J., Kontos, Christopher D., Cha, Eugene H., Prieto, Victor G., Shea, Christopher R., Berg, Jonathan N., Nevin, Norman C., Simpson, Sheila A., Pasyk, Krystyna A., Speer, Marcy C., Peters, Kevin G., Marchuk, Douglas A.

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Gene therapy advisory committee: long-term monitoring of patients participating in gene therapy: Health Departments of the United Kingdom von Nevin, Norman C, Spink, Jayne

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Genetic linkage of familial expansile osteolysis to chromosome 18q von Hughes, Anne E., Shearman, Amanda M., Weber, James L., Barr, R.John, Wallace, Richard G.H., Osterberg, Paul H., Nevin, Norman C., A.B.Mollan, Raymond

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What has happened to gene therapy? von Nevin, N C

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Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia von Greeves, Lindsey G, Patterson, Christopher C, Carson, Dennis J, Thom, Ruth, Wolfenden, Melanie C, Zschocke, Johannes, Graham, Colin A, Nevin, Norman C, Trimble, Elisabeth R

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The Epidemiology of Myotonic Dystrophy in Northern Ireland von Magee, Alex, Nevin, Norman C.

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Additional Glomangioma Families Link to Chromosome 1p: No Evidence for Genetic Heterogeneity von Calvert, Jennifer T., Burns, Shannon, Riney, Travis J., Sahoo, Trilochan, Orlow, Seth J., Nevin, Norman C., Haisley-Royster, Camille, Prose, Neil, Simpson, Sheila A., Speer, Marcy C., Marchuk, Douglas A.

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Peutz-Jeghers Syndrome von Morrison, Patrick J, Nevin, Norman C

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Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis von Reardon, W, Wilkes, D, Rutland, P, Pulleyn, L J, Malcolm, S, Dean, J C, Evans, R D, Jones, B M, Hayward, R, Hall, C M, Nevin, N C, Baraister, M, Winter, R M

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Experience of Gene Therapy in the United Kingdom von NEVIN, NORMAN C.

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Mutations in Keratin K9 in Kindreds with Epidermolytic Palmoplantar Keratoderma and Epidemiology in Northern Ireland von Covello, Seana P., Irvine, Alan D., McKenna, Kevin E., Munro, Colin S., Nevin, Norman C., Smith, Frances J.D., Uitto, Jouni, Irwin McLean, W.H.

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Female Germline Mosaicism in Tuberous Sclerosis Confirmed by Molecular Genetic Analysis von Yates, John R.W., van Bakel, Inge, Sepp, Tiina, Payne, Stewart J., Webb, David W., Nevin, Norman C., Green, Andrew J.

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Tumour necrosis factor microsatellites show association with multiple sclerosis von Kirk, Claire W., Droogan, Aidan G., Hawkins, Stanley A., McMillan, Stanley A., Nevin, Norman C., Graham, Colin A.

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Phenylketonuria and the peoples of Northern Ireland von ZSCHOCKE, J, MALLORY, J. P, EIKEN, H. G, NEVIN, N. C

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Phenylketonuria mutation analysis of Northern Ireland : a rapid stepwise approach von ZSCHOCKE, J, GRAHAM, C. A, CARSON, D. J, NEVIN, N. C

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In utero gene therapy von Nevin, Norman C

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NEUROPATHOLOGICAL CHANGES IN THE WHITE MATTER FOLLOWING HEAD INJURY von NEVIN, NORMAN C

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Advances in Genetics: Spiralling into Trouble? von Nevin, Norman C

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A Novel Mutation in the Helix Termination Peptide of Keratin 5 Causing Epidermolysis Bullosa Simplex Dowling–Meara von Irvine, Alan D., McKenna, Kevin E., Bingham, Anne, Nevin, Norman C., Hughes, Anne E.

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Cloning von Nevin, Norman C, Regan, Lesley

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