Molecular mapping of alzheimer-type dementia in Down's syndrome von Prasher, V. P., Farrer, Matthew J., Kessling, Anna M., Fisher, Elizabeth M. C., West, R. J., Barber, P. C., Butler, A. C.

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MTHFR association with arteriosclerotic vascular disease? von FLETCHER, O, KESSLING, A. M

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Association of the TNF-α-308 (G→A) polymorphism with self-reported history of childhood asthma von WINCHESTER, Elizabeth C, MILLWOOD, Iona Y, RAND, Lucinda, PENNY, Michelle A, KESSLING, Anna M

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Mortality in Women with Turner Syndrome in Great Britain: A National Cohort Study von Schoemaker, Minouk J., Swerdlow, Anthony J., Higgins, Craig D., Wright, Alan F., Jacobs, Patricia A.

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Maternal leptin receptor gene variant Gln223Arg is not associated with variation in birth weight or maternal body mass index in UK and South Asian populations von RAND, L, WINCHESTER, E. C, MILLWOOD, I. Y, PENNY, M. A, KESSLING, A. M

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The expression of PAX5 in human transitional cell carcinoma of the bladder: relationship with de‐differentiation von ADSHEAD, J. M, OGDEN, C. W, PENNY, M. A, STUART, E. T, KESSLING, A. M

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Purification, properties, and diagnosis of banana bract mosaic potyvirus and its distinction from abaca mosaic potyvirus von THOMAS, J. E, GEERING, A. D. W, GAMBLEY, C. F, KESSLING, A. F, WHITE, M

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Sources of Variation in Plasma Lipid and Lipoprotein Traits in a Sample Selected for Health von Lussier-Cacan, Suzanne, Xhignesse, Marianne, Kessling, Anna M., Davignon, Jean, Sing, Charles F.

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Survivin gene expression and prognosis in recurrent colorectal cancer von Miller, M, Smith, D, Windsor, A, Kessling, A

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Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? von BAPTISTA, Melisa J, FAIRBROTHER, Una L, KESSLING, Anna M, HOWARD, Catherine M, FARRER, Matthew J, DAVIES, Gail E, TRIKKA, Dimitra, MARATOU, Klio, REDINGTON, Andrew, GREVE, Gottfried, NJØLSTAD, Pal Rasmus

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Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-... von Bétard, Christine, Kessling, A.M., Roy, M., Davignon, J.

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Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent von Minnich, A, Kessling, A, Roy, M, Giry, C, DeLangavant, G, Lavigne, J, Lussier-Cacan, S, Davignon, J

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Novel Methodology for the Detection of Chromosome 21-Specific α-Satellite DNA Sequences von Maratou, Klio, Siddique, Yasmeen, Kessling, Anna M., Davies, Gail E.

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Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome von Farrer, Matthew J, Crayton, Lissa, Davies, Gail E, Oliver, Christopher, Powell, John, Holland, Anthony J, Kessling, Anna M

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Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health von Xhignesse, M, Lussier-Cacan, S, Sing, C F, Kessling, A M, Davignon, J

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Human COL6A1: Genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2 von Trikka, D, Davis, T, Lapenta, V, Brahe, C, Kessling, A M

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MOLECULAR GENETIC-EVIDENCE FOR A FOUNDER EFFECT IN FAMILIAL HYPERCHOLESTEROLEMIA AMONG FRENCH-CANADIANS von BETARD, C, KESSLING, AM, ROY, M, CHAMBERLAND, A, LUSSIERCACAN, S, DAVIGNON, J

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Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction von MARATOU, K, SIDDIQUE, Y, KESSLING, A. M, DAVIES, G. E

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Genetic initiation, progression and prognostic markers in transitional cell carcinoma of the bladder: a summary of the structural and transcriptional changes, and the role of devel... von ADSHEAD, J. M, KESSLING, A. M, OGDEN, C. W

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Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster von HAVILAND, M. B, KESSLING, A. M, DAVIGNON, J, SING, C. F

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