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Results: 1-6 |
Results: 6

Authors: Mosig, G Gewin, J Luder, A Colowick, N Vo, D
Citation: G. Mosig et al., Two recombination-dependent DNA replication pathways of bacteriophage T4, and their roles in mutagenesis and horizontal gene transfer, P NAS US, 98(15), 2001, pp. 8306-8311

Authors: Mandel, H Abeling, N Gutman, A Berant, M Scholten, EG Sheiman, C Luder, A van Gennip, AH
Citation: H. Mandel et al., Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis, PRENAT DIAG, 20(11), 2000, pp. 927-929

Authors: Shatzky, S Moses, S Levy, J Pinsk, V Hershkovitz, E Herzog, L Shorer, Z Luder, A Parvari, R
Citation: S. Shatzky et al., Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: Genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies, AM J MED G, 92(5), 2000, pp. 353-360

Authors: Koren, A Segal-Kupershmit, D Zalman, L Levin, C Abu Hana, M Palmor, H Luder, A Attias, D
Citation: A. Koren et al., Effect of hydroxyurea in sickle cell anemia: A clinical trial in children and teenagers with severe sickle cell anemia and sickle cell beta-thalassemia, PED HEM ONC, 16(3), 1999, pp. 221-232

Authors: Bercovich, D Regev, Z Ratz, T Luder, A Plotsky, Y Gruenbaum, Y
Citation: D. Bercovich et al., Quantitative ratio of primer pairs and annealing temperature affecting PCRproducts in duplex amplification, BIOTECHNIQU, 27(4), 1999, pp. 762

Authors: Klose, A Peters, H Hoffmeyer, S Buske, A Luder, A Hess, D Lehmann, R Nurnberg, P Tinschert, S
Citation: A. Klose et al., Two independent mutations in a family with neurofibromatosis type 1 (NF1), AM J MED G, 83(1), 1999, pp. 6-12
Risultati: 1-6 |