Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 von Robin, Nathaniel H., Feldman, George J., Aronson, Adam L., Mitchell, Heather F., Weksberg, Rosanna, Leonard, Claire O., Burton, Barbara K., Josephson, Kevin D., Laxová, Renata, Aleck, Kyrieckos A., Allanson, Judith E., Guion-Almeida, Maria Leine, Martin, Rick A., Leichtman, Lawrence G., Price, R. Arlen, Opitz, John M., Muenke, Maximilian

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Simultaneous usage of homologous points, lines, and planes for optimal, 3-D, linear registration of multimodality imaging data von Meyer, C.R., Leichtman, G.S., Brunberg, J.A., Wahl, R.L., Quint, L.E.

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Cyclosporin for severe ulcerative colitis von Naftali, T, Novis, B, Pomeranz, I, Leichtman, G, Maor, Y, Shapiro, R, Moskowitz, M, Avidan, B, Avni, Y, Bujanover, Y, Fireman, Z

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Are cardio-facio-cutaneous syndrome and Noonan syndrome distinct? A case of CFC offspring of a mother with Noonan syndrome von Leichtman, L G

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Expression of bcl-2 in autoimmune and Helicobacter pylori-associated atrophic gastritis von MAOR-KENDLER, Y, GABAY, G, BERNHEIM, J, NAFTALI, T, LESIN, I, LEICHTMAN, G, POMERANZ, I, NOVIS, B

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Spontaneous intramural esophageal hemorrhage von Elis, A, Zissin, R, Leichtman, G, Lishner, M

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Automated Gamma Knife dose planning using polygon clipping and adaptive simulated annealing von Leichtman, Gregg S., Aita, Anthony L., Goldman, H. Warren

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Pancreatic cancer in Israel: the epidemiology, possibilities of prevention, early detection and screening von Rozen, Paul, Liphshitz, Irena, Rosner, Guy, Barchana, Micha, Lachter, Jesse, Pel, Sara, Shohat, Tami, Santo, Erwin

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A Comparative Study of Metronidazole and Sulfasalazine in Active, Not Severe, Ulcerative Colitis: An Israeli Multicenter Trial von Gilat, T, Suissa, A, Leichtman, G, Delpre, G, Pavlotzky, M, Grossman, A, Fireman, Z

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Apparent Opitz BBBG syndrome with a partial duplication of 5p von Leichtman, Lawrence G., Werner, Alice, Bass, W. Thomas, Smith, Deborah, Brothman, Arthur R.

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A Comparison of Metronidazole and Sulfasalazine in the Maintenance of Remission in Patients with Ulcerative Colitis von Gilat, T, Leichtman, G, Delpre, G, Eshchar, J, Meir, S Bar, Fireman, Z

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Anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder in a newborn: A midline developmental field defect von Leichtman, Lawrence G., Wood, Brian, Rohn, Reuben

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Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25) von Leichtman, Lawrence G., Strum, Daniel, Brothman, Arthur R.

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Further delineation of Weaver syndrome von Ardinger, Holly H., Hanson, James W., Harrod, Mary Jo E., Cohen, M. Michael, Tibbles, John A.R., Welch, J. Philip, Young-Wee, Theresa, Sommer, Annemarie, Goldberg, Rosalie, Shprintzen, Robert J., Sidoti, Eugene J., Leichtman, Lawrence G., Hoyme, H. Eugene

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Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9p von Leichtman, Lawrence G., Zackowski, Joleen L., Storto, Patrick D., Newlin, Anna

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Secondary aortoduodenal fistula von Witz, Misha, Lehmann, Jonathan M, Shnaker, Ali, Pomeranz, Itamar, Leichtman, George, Novis, Benthly

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An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome? von Carpenter, N J, Leichtman, L G, Stamper, S, Say, B

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Primary pulmonary hypoplasia and arthrogryposis multiplex congenita von Leichtman, Lawrence G., Say, Burhan, Barber, Nancy

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The Gordon syndrome von Say, B, Barber, D H, Thompson, R C, Leichtman, L G

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Patients in a clinic for children with multiple handicaps: a retrospective diagnostic evaluation von Leichtman, L G, Say, B, Coldwell, J G

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