Neuropsychiatric symptomatology predicts seizure recurrence in newly treated patients von PETROVSKI, S, SZOEKE, C. E. I, JONES, N. C, SALZBERG, M. R, SHEFFIELD, L. J, HUGGINS, R. M, O'BRIEN, T. J

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Follow up and evaluation of the Victorian first‐trimester combined screening programme for Down syndrome and trisomy 18 von Jaques, AM, Halliday, JL, Francis, I, Bonacquisto, L, Forbes, R, Cronin, A, Sheffield, LJ

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Pharmacogenomics Education: International Society of Pharmacogenomics Recommendations for Medical, Pharmaceutical, and Health Schools Deans of Education von Gurwitz, D, Lunshof, J E, Dedoussis, G, Flordellis, C S, Fuhr, U, Kirchheiner, J, Licinio, J, Llerena, A, Manolopoulos, V G, Sheffield, L J, Siest, G, Torricelli, F, Vasiliou, V, Wong, S

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Familial temporal lobe epilepsy: A common disorder identified in twins von Berkovic, Samuel F., McIntosh, Anne, Howell, R. Anne, Mitchell, Anne, Sheffield, Leslie J., Hopper, John L.

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Randomized double‐blind placebo‐controlled crossover study to determine the effects of esomeprazole on inhibition of platelet function by clopidogrel von FERNANDO, H., BASSLER, N., HABERSBERGER, J., SHEFFIELD, L. J., SHARMA, R., DART, A. M., PETER, K. H., SHAW, J. A.

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Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications von Wincent, J., Bruno, D.L., van Bon, B.W.M., Bremer, A., Stewart, H., Bongers, E.M.H.F., Ockeloen, C.W., Willemsen, M.H., Keays, D.A.D., Baird, G., Newbury, D.F., Kleefstra, T., Marcelis, C., Kini, U., Stark, Z., Savarirayan, R., Sheffield, L.J., Zuffardi, O., Slater, H.R., de Vries, B.B., Knight, S.J.L., Anderlid, B.-M., Schoumans, J.

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A low allergen diet is a significant intervention in infantile colic: Results of a community-based study von Hill, David J., Hudson, Irene L., Sheffield, Leslie J., Shelton, Michael J., Menahem, Samuel, Hosking, Clifford S.

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An Ultrasound Renal Cyst Prevalence Survey: Specificity Data for Inherited Renal Cystic Diseases von Ravine, David, Gibson, Robert N., Donlan, John, Sheffield, Leslie J.

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Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1 von Ravine, D., Sheffield, Lj, Danks, D.M., Gibson, R.N., Walker, R.G., Kincaid-Smith, P.

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Asymmetry and skin pigmentary anomalies in chromosome mosaicism von Woods, C G, Bankier, A, Curry, J, Sheffield, L J, Slaney, S F, Smith, K, Voullaire, L, Wellesley, D

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Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata von Sheffield, L J, Osborn, A H, Hutchison, W M, Sillence, D O, Forrest, S M, White, S J, Dahl, H H

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Importance of complete follow-up of spontaneous fetal loss after amniocentesis and chorion villus sampling von Halliday, J.L., Sheffield, L.J., Lumley, J., Robinson, H.P., Renou, P., Carlin, J.B.

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Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease von Ravine, D, Forrest, S.M, Sheffield, L.J, Danks, D.M, Walker, R.G, Kincaid-Smith, P, Gibson, R.N, Richards, R.I., Friend, K.

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Screening approach for Fragile X syndrome von Delatycki, M. B., Sheffield, L. J., Wake, S., Cohen, J.

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New estimates of down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population von Halliday, Jane L., Watson, Lyndsey F., Lumley, Judith, Danks, David M., Sheffield, Leslie J.

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Fetal outcome and maternal morbidity after early amniocentesis von Collins, V. R., Webley, C., Sheffield, L. J., Halliday, J. L.

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The elusive Angelman syndrome critical region von Trent, R J, Sheffield, L J, Deng, Z M, Kim, W S, Nassif, N T, Ryce, C, Woods, C G, Michaelis, R C, Tarleton, J, Smith, A

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Analyses of the COGA data set in one ethnic group with examinations of alternative definitions of alcoholism von Sheffield, L.J., Knauert, M.P., Pakstis, A.J., Zhao, H., Kidd, K.K.

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Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease von Ravine, D., Sheffield, L.J., Danks, D.M., Walker, R.G., Kincaid-Smith, P., Gibson, Rn

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Maxillonasal dysplasia (Binder's syndrome) and chondrodysplasia punctata von Sheffield, L J, Halliday, J L, Jensen, F

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