How valid and accurate are measurements of golf impact parameters obtained using commercially available radar and stereoscopic optical launch monitors? von Leach, R.J., Forrester, S.E., Mears, A.C., Roberts, J.R.

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Case Report: Syndrome of Remitting Seronegative Symmetrical Synovitis with Pitting Edema—A Rare but Treatable Condition in Palliative Medicine von Moore, L Merkle, Brouner, Jennifer M, Grigorian, Nelly, Leach, R J, Baumrucker, Steven J

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The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication von Vance, J.M, Van Broeckhoven, C, Timmerman, V, Othman, K. Ben, Nieuwenhuijsen, B.W, Chen, K.L, Wang, S, Raeymaekers, P, Van Hul, W, van Ommen, G-J.B, Hanemann, C.O, Müller, H.W, Martin, J-J, Leach, R.J, Fischbeck, K.H, De Jonghe, P, Cullen, B, Nelis, E

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Effects of combining transforming growth factor beta and 1,25-dihydroxyvitamin D3 on differentiation of a human osteosarcoma (MG-63) von BONEWALD, LF, KESTER, MB, SCHWARTZ, Z, SWAIN, LD, KHARE, A, JOHNSON, TL, LEACH, RJ, BOYAN, BD

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Genetic Linkage of the Dentinogenesis Imperfecta Type III Locus to Chromosome 4q von MacDougall, M., Jeffords, L.G., Gu, T.T., Knight, C.B., Frei, G., Reus, B.E., Otterud, B., Leppert, M., Leach, R.J.

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TGFB-induced factor (TGIF): a candidate gene for psychosis on chromosome 18p von CHAVARRIA-SILES, I, WALSS-BASS, C, RAVENTOS, H, ESCAMILLA, M. A, QUEZADA, P, DASSORI, A, CONTRERAS, S, MEDINA, R, RAMIREZ, M, ARMAS, R, SALAZAR, R, LEACH, R. J

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Genetic Linkage of Paget Disease of the Bone to Chromosome 18q von Cody, J.D., Singer, F.R., Roodman, G.D., Otterund, B., Lewis, T.B., Leppert, M., Leach, R.J.

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Preliminary Models of the Cost of Fault Tolerance von Leach, R.J.

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Genetic heterogeneity in benign familial neonatal convulsions : identification of a new locus on chromosome 8q von LEWIS, T. B, LEACH, R. J, WARD, K, O'CONNELL, P, RYAN, S. G

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Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q von CODY, J. D, REVELES, X. T, HALE, D. E, LEHMAN, D, COON, H, LEACH, R. J

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Assignment 1 of OSTF1 to human chromosome bands 12q24.1→q24.2 by in situ hybridization von Schaub, R., Dupont, B., Roodman, G.D., Leach, R.J., Reddy, S.V.

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Genetic mapping of a novel X-linked recessive colobomatous microphthalmia von Lehman, D.M., Sponsel, W.E., Stratton, R.F., Mensah, J., Macdonald, J.C., Johnson-Pais, T.L., Coon, H., Reveles, X.T., Cody, J.D., Leach, R.J.

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Chromosome 18 suppresses prostate cancer metastases von Padalecki, S.S., Weldon, K.S., Reveles, X.T., Buller, C.L., Grubbs, B., Cui, Y., Yin, J.J., Hall, D.C., Hummer, B.T., Weissman, B.E., Dallas, M., Guise, T.A., Leach, R.J., Johnson-Pais, T.L.

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Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q von Cody, J.D., Reveles, X.T., Hale, D.E., Lehman, D., Coon, H., Leach, R.J.

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A small paracentric inversion of chromosome 18, inv(18) (q22.1q23), in a woman with multiple congenital anomalies and mental retardation von Sekhon, G.S., Scheib-Wixted, S., Williams, M.S., Reveles, X.T., Leach, R.J.

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Work in progress - knowledge engineering in a hybrid systems engineering curriculum von Leach, R.J., Keeling, H.N.

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Localization of a Gene for a Glutamate Binding Subunit of a NMDA Receptor (GRINA) to 8q24 von Lewis, T.B., Wood, S., Michaelis, E.K., DuPont, B.R., Leach, R.J.

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Experiments in software reengineering von Leach, R.J.

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Regions of allelic imbalance in the distal portion of chromosome 12q in gastric cancer von Schneider, B G, Rha, S Y, Chung, H C, Bravo, J C, Mera, R, Torres, J C, Plaisance, K T, Schlegel, R, McBride, C M, Reveles, X T, Leach, R J

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Regional Localization of 188 Sequence Tagged Sites on a Somatic Cell Hybrid Mapping Panel for Human Chromosome 3 von Leach, R.J., Chinn, R., Reus, B.E., Hayes, S., Schantz, L., Dubois, B., Overhauser, J., Ballabio, A., Drabkin, H., Lewis, T.B., Mendgen, G., Naylor, S.L.

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