Prediction of Propulsion Kinematics and Performance in Wheelchair Rugby von Haydon, David S., Pinder, Ross A., Grimshaw, Paul N., Robertson, William S. P., Holdback, Connor J. M.

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Fenceline contact of beef calves with their dams at weaning reduces the negative effects of separation on behavior and growth rate von Price, E. O, Harris, J. E, Borgwardt, R. E, Sween, M. L, Connor, J. M

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Leveraging Pyrazolium Ylide Reactivity to Access Indolizine and 1,2‐Dihydropyrimidine Derivatives von Tran, Ricky, Brownsey, Duncan K., O'Sullivan, Leonie, Brandow, Connor M. J., Chang, Emily S., Zhou, Wen, Patel, Ketul V., Gorobets, Evgueni, Derksen, Darren J.

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Long term follow up of nasolacrimal intubation in adults von Connell, P P, Fulcher, T P, Chacko, E, O’ Connor, M J, Moriarty, P

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First-trimester combined ultrasound and biochemical screening for Down syndrome in routine clinical practice von Stenhouse, E. J., Crossley, J. A., Aitken, D. A., Brogan, K., Cameron, A. D., Connor, J. M.

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Would you dope? A general population test of the Goldman dilemma von Connor, J M, Mazanov, J

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Methylene tetrahydrofolate reductase (MTHFR) and nitric oxide synthase (ecNOS) genes and risks of peripheral arterial disease and coronary heart disease: Edinburgh artery study von Fowkes, F.G.R, Lee, A.J, Hau, C.M, Cooke, A, Connor, J.M, Lowe, G.D.O

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Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins von Johnson, D, Morrison, N, Grant, L, Turner, T, Fantes, J, Connor, J M, Murday, V

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CDKN2A Germline Mutations in U.K. Patients with Familial Melanoma and Multiple Primary Melanomas von MacKie, Rona M., Andrew, Nicola, Lanyon, W.G., Connor, J.M.

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The Angiotensin I Converting Enzyme Gene and Predisposition to High Blood Pressure von Harrap, Stephen B, Davidson, H Rosemarie, Connor, J Michael, Soubrier, Florent, Corvol, Pierre, Fraser, Robert, Foy, Chris J.W, Watt, Graham C.M

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Essential Medical Genetics von Tobias, Edward S, Connor, Michael, Smith, Malcolm Ferguson

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Neuroticism and polymorphisms in the serotonin transporter gene von DEARY, I. J., BATTERSBY, S., WHITEMAN, M. C., CONNOR, J. M., FOWKES, F. G. R., HARMAR, A.

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Fibrodysplasia Ossificans Progressiva, a Heritable Disorder of Severe Heterotopic Ossification, Maps to Human Chromosome 4q27-31 von Feldman, George, Li, Ming, Martin, Shelden, Urbanek, Margrit, Urtizberea, J. Andoni, Fardeau, Michel, LeMerrer, Martine, Connor, J. Michael, Triffitt, James, Smith, Roger, Muenke, Maximilian, Kaplan, Frederick S., Shore, Eileen M.

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Dimeric Inhibin A as a Marker for Down's Syndrome in Early Pregnancy von Aitken, David A, Wallace, Euan M, Crossley, Jennifer A, Swanston, Ian A, van Pareren, Yvonne, van Maarle, Merel, Groome, Nigel P, Macri, James N, Connor, J. Michael

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The chromosome constitution of human preimplantation embryos fertilized in vitro von Jamieson, M.E., Coutts, J.R.T., Connor, J.M.

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Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region von Arngrímsson, Reynir, Hayward, Caroline, Nadaud, Sophie, Baldursdóttir, Asdis, Walker, James J., Liston, Wang A., Bjarnadóttir, Ragnheiür I., Brock, David J.H., Geirsson, Reynir T., Connor, J. Michael, Soubrier, Florent

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Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP) von Xu, M-Q, Feldman1, G, Le Merrer, M, Shugart, YY, Glaser, DL, Urtizberea, JA, Fardeau, M, Connor, JM, Triffitt, J, Smith, R, Shore, EM, Kaplan, FS

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Maternal smoking: age distribution, levels of alpha-fetoprotein and human chorionic gonadotrophin, and effect on detection of Down syndrome pregnancies in second-trimester screenin... von Crossley, J. A., Aitken, D. A., Waugh, S. M. L., Kelly, T., Connor, J. M.

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Fibrinogen genotype and risk of peripheral atherosclerosis von Fowkes, F.G.R, Smith, F.B, Donnan, P.T, Connor, J.M, Wood, J, Lowe, G.D.O

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Genetic aspects of tuberous sclerosis in the west of Scotland von Sampson, J R, Scahill, S J, Stephenson, J B, Mann, L, Connor, J M

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