Early Gastric Cancer in Young, Asymptomatic Carriers of Germ-Line E-Cadherin Mutations von Huntsman, David G, Carneiro, Fatima, Lewis, Frank R, MacLeod, Patrick M, Hayashi, Allen, Monaghan, Kristin G, Maung, Raymond, Seruca, Raquel, Jackson, Charles E, Caldas, Carlos

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The man behind the honors Dr. P. M. MacLeod MD FRCPC FCCMG DABG von MacLeod, Patrick M.

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SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases von Colijn, Mark A., Carrion, Prescilla, Poirier-Morency, Guillaume, Rogic, Sanja, Torres, Ivan, Menon, Mahesh, Lisonek, Michelle, Cook, Courtney, DeGraaf, Ashley, Thammaiah, Subramanya Ponnachana, Neelakant, Harish, Willaeys, Veerle, Leonova, Olga, White, Randall F., Yip, Stephen, Mungall, Andrew J., MacLeod, Patrick M., Gibson, William T., Sullivan, Patrick F., Honer, William G., Pavlidis, Paul, Stowe, Robert M.

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Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme von Brown, N F, Mullur, R S, Subramanian, I, Esser, V, Bennett, M J, Saudubray, J M, Feigenbaum, A S, Kobari, J A, Macleod, P M, McGarry, J D, Cohen, J C

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Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy von Thibodeau, My Linh, Peters, Colin H., Townsend, Katelin N., Shen, Yaoqing, Hendson, Glenda, Adam, Shelin, Selby, Kathryn, Macleod, Patrick M., Gershome, Cynthia, Ruben, Peter, Jones, Steven J. M., Friedman, Jan M., Gibson, William T., Horvath, Gabriella A.

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A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome von Minassian, Berge A, Mnatzakanian, Gevork N, Lohi, Hannes, Munteanu, Iulia, Alfred, Simon E, Yamada, Takahiro, MacLeod, Patrick J M, Jones, Julie R, Scherer, Stephen W, Schanen, N Carolyn, Friez, Michael J, Vincent, John B

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Inverted duplication with terminal deletion of 5p and no cat‐like cry von Wang, Jia‐Chi, Coe, Bradley P., Lomax, Brenda, MacLeod, Patrick M., Parslow, Malcolm I., Schein, Jacqueline E., Lam, Wan L., Eydoux, Patrice

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Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients von Wang, Jia-Chi, Dang, Linda, Lomax, Brenda, Turner, Lesley, Shago, Mary, Teebi, Ahmad S., Klatt, Regan, MacLeod, Patrick M., Yong, Siu-Li, Nowaczyk, Malgorzata J.M., Eydoux, Patrice

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A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD von Boycott, Kym M., Parslow, Malcolm I., Ross, Judith L., Miller, Ivan P., Bech‐Hansen, N. Torben, MacLeod, Patrick M.

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Longevity in Rett Syndrome: Analysis of the North American Database von Kirby, Russell S., PhD, Lane, Jane B., BSN, Childers, Jerry, Skinner, Steve A., MD, Annese, Fran, LMSW, Barrish, Judy O., BSN, Glaze, Daniel G., MD, MacLeod, Patrick, MD, Percy, Alan K., MD

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Inherited Mutations in PTEN That Are Associated with Breast Cancer, Cowden Disease, and Juvenile Polyposis von Lynch, Eric D., Ostermeyer, Elizabeth A., Lee, Ming K., Arena, J. Fernando, Ji, HanLee, Dann, Jamie, Swisshelm, Karen, Suchard, David, MacLeod, Patrick M., Kvinnsland, Stener, Gjertsen, Bjorn Tore, Heimdal, Ketil, Lubs, Herb, Møller, Pål, King, Mary-Claire

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Evidence for multi-site closure of the neural tube in humans von Van Allen, Margot I., Kalousek, Dagmar K., Chernoff, Gerold F., Juriloff, Diana, Harris, Muriel, McGillivray, Barbara C., Yong, Siu-Li, Langlois, Sylvie, Macleod, Patrick M., Chitayat, David, Friedman, Jan M., Wilson, R. Doug, McFadden, Deborah, Pantzar, J., Ritchie, Susan, Hall, Judith G.

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Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease von Tan, Charles C., Ainsworth, Peter J., Hahn, Angelika F., MacLeod, Patrick M.

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Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus von Twist, E C, Casaubon, L K, Ruttledge, M H, Rao, V S, Macleod, P M, Radvany, J, Zhao, Z, Rosenberg, R N, Farrer, L A, Rouleau, G A

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A Canadian CADASIL Kindred: How sensitive is a skin biopsy? von Demaerschalk, Bart, MacLeod, Patrick M, Lee, Donald H, Hammond, Robert R, Ainsworth, Peter J, Musyj, Sherry K, Hachinski, Vladimir

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Growth and development in thanatophoric dysplasia von MacDonald, Ian M., Hunter, Alasdair G. W., MacLeod, Patrick M., MacMurray, S. Brock

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Recurrent respiratory infections in a child with fucosidosis: Is the mucus too thin for effective transport? von Rubin, Bruce K., Macleod, Patrick M., Sturgess, Jennifer, King, Malcolm

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Drs. Robertson and MacLeod reply von Robertson, Rocke, MacLeod, Patrick M.

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Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus von TWIST, E. C, FARRER, L. A, MACLEOD, P. M, RADVANY, J, CHAMBERLAIN, S, ROSENBERG, R. N, ROULEAU, G. A

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The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1) von Carson, Wendy J., Radvany, Joao, Farrer, Lindsay A., Vincent, Dominique, Rosenberg, Roger N., MacLeod, Patrick M., Rouleau, Guy A.

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