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Sprecher, E
Bergman, R
Richard, G
Lurie, R
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Petronius, D
Shalata, A
Anbinder, Y
Leibu, R
Perlman, I
Cohen, N
Szargel, R
Citation: E. Sprecher et al., Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin, NAT GENET, 29(2), 2001, pp. 134-136
Authors:
Herman, MG
Balter, JM
Jaffray, DA
McGee, KP
Munro, P
Shalev, S
Van Herk, M
Wong, JW
Citation: Mg. Herman et al., Clinical use of electronic portal imaging: Report of AAPM radiation therapy committee Task Group 58, MED PHYS, 28(5), 2001, pp. 712-737
Authors:
Levin, C
Zalman, L
Shalev, S
Mader, R
Koren, A
Citation: C. Levin et al., Legg-Calve-Perthes disease, protein C deficiency, and beta-thalassemia major: Report of two cases, J PED ORTH, 20(1), 2000, pp. 129-131
Authors:
Shalata, A
Mandel, H
Dorche, C
Zabot, MT
Shalev, S
Hugeirat, Y
Arieh, D
Ronit, Z
Reiss, J
Anbinder, Y
Cohen, N
Citation: A. Shalata et al., Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in Northern Israel using polymorphic DNA markers, PRENAT DIAG, 20(1), 2000, pp. 7-11
Authors:
Zlotogora, J
Shalev, S
Habiballah, H
Barjes, S
Citation: J. Zlotogora et al., Genetic disorders among Palestinian Arabs: 3. Autosomal recessive disorders in a single village, AM J MED G, 92(5), 2000, pp. 343-345
Citation: S. Shalev et al., Nails from a 2,400 year old shipwreck: A study of copper in a marine archaeological environment, JOM-J MIN, 51(2), 1999, pp. 14
Authors:
Koren, A
Zalman, L
Levin, C
Abu Hana, M
Mader, R
Shalev, S
Citation: A. Koren et al., Venous thromboembolism, factor V Leiden, and methylenetetrahydrofolate reductase in a sickle cell anemia patient, PED HEM ONC, 16(5), 1999, pp. 469-472