Apparent prevention of neural tube defects by periconceptional vitamin supplementation von Smithells, RW, Sheppard, S, Schorah, CJ, Seller, MJ, Nevin, NC, Harris, R, Read, AP, Fielding, DW

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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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Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome) von Morrison, P J, Nevin, N C

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Familial primary spontaneous pneumothorax consistent with true autosomal dominant inheritance von Morrison, P J, Lowry, R C, Nevin, N C

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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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ACE gene typing von Fogarty, D.G., Maxwell, A.P., Doherty, C.C., Hughes, A.E., Nevin, N.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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The epidemiology of Huntington's disease in Northern Ireland von Morrison, P J, Johnston, W P, Nevin, N C

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Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities von Grimshaw, G M, Szczepura, A, Hultén, M, MacDonald, F, Nevin, N C, Sutton, F, Dhanjal, S

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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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A supernumerary chromosome 20, identified by FISH, in a male with azoospermia-cause or coincidence? von McNerlan, S.E., Morrison, Patrick J., McClure, N., Nevin, N.C.

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Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland von Dean, G, Nevin, N C, Mikkelsen, M, Karadima, G, Petersen, M B, Kelly, M, O'Sullivan, J

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

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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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Laryngeal atresia or stenosis presenting as second-trimester fetal ascites-diagnosis and pathology in three independent cases von Morrison, P. J., MacPhail, S., Williams, D., McCusker, G., McKeever, P., Wright, C., Nevin, N. 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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The prevalence of inherited neuromuscular disease in Northern Ireland von Hughes, M.I., Hicks, E.M., Nevin, N.C., Patterson, V.H

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Evidence for a second genetic locus in Carney complex von IRVINE, A. D, ARMSTRONG, D. K. B, BINGHAM, E. A, HADDEN, D. R, NEVIN, N. C, HUGHES, A. E

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De novo direct duplication 2 (p12 p21) with paternally inherited pericentric inversion 2p11.2 2q12.2 von Magee, A. C., Humphreys, M. W., McKee, S., Stewart, M., Nevin, N. C.

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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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