Genetic Service Delivery: Infrastructure, Assessment and Information von Kaye, C.I.

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Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome : Evidence for myelin basic protein haploinsufficiency von GAY, C. T, HARDIES, L. J, SCHIFF, J. M, KAYE, C. I, LEACH, R. J, FOX, P. T, RAUCH, R. A, LANCASTER, J. L, PLAETKE, R, DUPONT, B. R, CODY, J. D, CORNELL, J. E, HERNDON, R. C, GHIDONI, P. D

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Health Care Supervision for Children With Williams Syndrome von Cunniff, Christopher, Frias, Jaime L, Kaye, Celia I, Moeschler, John

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Evaluation of the Newborn With Developmental Anomalies of the External Genitalia von Kaye, Celia I, Cunniff, Christopher, Frias, Jaime L, Moeschler, John

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Rumination risk of aspiration of gastric contents in the Prader-Willi syndrome von SLOAN, T. B, KAYE, C. I

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Multiple organ dysfunction after trauma von Cole, E, Gillespie, S, Vulliamy, P, Brohi, K, Akkad, H, Apostolidou, K, Ardley, R, Aylwin, C, Bassford, C, Bonner, S, Brooks, A, Cairns, T, Cecconi, M, Clark, F, Dempsey, G, Denison Davies, E, Docking, R, Eddlestone, J, Ellis, D, Evans, J, Galea, M, Healy, M, Horner, D, Howarth, R, Jansen, J, Jones, J, Kaye, C, Keep, J, Kerslake, D, Kilic, J, Leong, M, Martinson, V, McIldowie, B, Michael, S, Millo, J, Morgan, M, O'Leary, R, Oram, J, Ortiz-Ruiz De Gordoa, L, Porter, K, Raby, S, Service, J, Shaw, D, Smith, J D, Smith, N, Stotz, M, Thomas, E, Thomas, M, Vincent, A, Ward, G, Welters, I

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Outcomes of interest in evidence-based evaluations of genetic tests von Botkin, Jeffrey R., Teutsch, Steven M., Kaye, Celia I., Hayes, Maxine, Haddow, James E., Bradley, Linda A., Szegda, Kathleen, Dotson, W. David

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Oculoauriculovertebral anomaly: Segregation analysis von Kaye, Celia I., Martin, Alice O., Rollnick, Beverly R., Rollnick, R., Nagatoshi, Konrad, Israel, Jeannette, Hermanoff, Mark, Tropea, Brad, Richtsmeier, Joan T., Morton, Newton E.

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Measuring Contributions to the Research Mission of Medical Schools von Holmes, Edward W, Burks, Thomas F, Dzau, Victor, Hindery, Michael A, Jones, Robert F, Kaye, Celia I, Korn, David, Limbird, Lee E, Marchase, Richard B, Perlmutter, Roger, Sanfilippo, Fred, Strom, Brian L

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Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q von Cody, Jannine D., Davis Ghidoni, Patricia, DuPont, Barbara R., Hale, Daniel E., Hilsenbeck, Susan G., Stratton, Robert F., Hoffman, Douglas S., Muller, Shaine, Schaub, Rebecca L., Leach, Robin J., Kaye, Celia I.

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Oculoauriculovertebral dysplasia and variants: Phenotypic characteristics of 294 patients von Rollnick, Beverly R., Kaye, Celia I., Nagatoshi, Konrad, Hauck, Walter, Martin, Alice O., Reynolds, James F.

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GENETICS EDUCATION FOR PRIMARY CARE PROVIDERS IN COMMUNITY HEALTH SETTINGS von Kolb, Sara E., Aguilar, Maricela C., Dinenberg, Maura, Kaye, Celia I.

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Membranous nephropathy in two human leukocyte antigen-identical brothers von Elshihabi, Ihsan, Kaye, Celia I., Brzowski, Anita

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Ganglioneuroblastoma and fetal hydantoin-alcohol syndromes von Seeler, R A, Israel, J N, Royal, J E, Kaye, C I, Rao, S, Abulaban, M

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Oculoauriculovertebral spectrum: an updated critique von Cohen, Jr, M M, Rollnick, B R, Kaye, C I

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Preferential loss of the paternal alleles in the 18q- syndrome von Cody, Jannine D., Pierce, Jessica F., Brkanac, Zoran, Plaetke, Rosemarie, Ghidoni, Patricia D., Kaye, Celia I., Leach, Robin J.

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Growth hormone insufficiency associated with haploinsufficiency at 18q23 von Cody, Jannine D., Hale, Daniel E., Brkanac, Zoran, Kaye, Celia I., Leach, Robin J.

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Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11) von Walter, Christi A., Shaffer, Lisa G., Kaye, Celia I., Huff, Robert W., Ghidoni, Patricia D., McCaskill, Christopher, McFarland, Melinda B., Moore, Charleen M.

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Mendelian inheritance of isolated nonsyndromic cleft palate von Rollnick, Beverly R., Kaye, Celia I., Opitz, John M., Reynolds, James F.

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Microtia and associated anomalies: Statistical analysis von Kaye, Celia I., Rollnick, Beverly R., Hauck, Walter W., Martin, Alice O., Richtsmeier, Joan T., Nagatoshi, Konrad

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