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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ACE gene typing von Fogarty, D.G., Maxwell, A.P., Doherty, C.C., Hughes, A.E., Nevin, N.C.

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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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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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A novel single base deletion in the LDLR gene (211delG): Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes von Ward, A.J., O'Kane, M., Nicholls, D.P., Young, I.S., Nevin, N.C., Graham, C.A.

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The KBG syndrome, characteristic dental findings: a case report von Dowling, P.A., Fleming, P., Gorlin, R.J., King, M., Nevin, N.C., McEntagart, M.

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Absence of PAX6 Gene Mutations in Gillespie Syndrome (Partial Aniridia, Cerebellar Ataxia, and Mental Retardation) von Glaser, Tom, Ton, Carl C.T., Mueller, Robert, Petzl-Erler, Maria Luiza, Oliver, Christina, Nevin, N.C., Housman, David E., Maas, Richard L.

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Exponential increase in the Huntington disease gene in a three-generation family von Morrison, P.J., Hill, A., McMenamin, J., Nevin, N.C.

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Lack of association between myelin basic protein gene microsatellite and multiple sclerosis von Graham, C.A., Kirk, C.W., Nevin, N.C., Droogan, A.G., Hawkins, S.A., Mcmillan, S.A., Mcneill, T.A.

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Apparent prevention of neural tube defects by periconceptional vitamin supplementation von Smithells, R W, Sheppard, S, Schorah, C J, Seller, M J, Nevin, N C, Harris, R, Read, A P, Fielding, D W

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Prevention of neural-tube-defect recurrences von Nevin, N.C., Seller, MaryJ

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The effect of biochemical and genetic lipid parameters on the clinical severity of familial hypercholesterolemia (FH) in a large N. Irish Family von Ward, A.J., O'Kane, M., Nevin, N.C., Nicholls, D.P., Graham, C.A.

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FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES von Smithells, R.W., Seller, M.J., Harris, R., Fielding, D.W., Schorah, C.J., Nevin, N.C., Sheppard, S., Read, A.P., Walker, S., Wild, J.

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PROLONGED COMA AFTER HEAD INJURY von Nevin, N.C.

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Prenatal diagnosis of mucolipidosis II by early amniocentesis von Besley, G.T.N., Broadhead, D.M., Nevin, N.C., Nevin, J., Dornan, J.C.

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Linkage analysis of Weber-Cockayne epidermolysis bullosa simplex von MCKENNA, K.E., HUGHES, A.E., MCLEAN, W.H.I., NEVIN, N.C.

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Chorionic villus sampling for Down's syndrome von Magee, A.C., Stewart, F.J., Nevin, J., Nevin, N.C., Dornan, J.C., Armstrong, M.J., Thornton, J.G.

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NEURAL TUBE DEFECTS von Nevin, N.C., Jongbloet, P.H.

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Presymptomatic screening for MEN-2A von Morrison, P.J., Nevin, N.C., Hughes, A.E., Hadden, D.R., Russell, C.F.J.

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PRODUCT LICENCE FOR PREGNAVITE FORTE F von Nevin, N.C., Seller, M.J., Smithells, R.W.

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