Authors: Meiner, V Shpitzen, S Mandel, H Klar, A Ben-Neriah, Z Zlotogora, J Sagi, M Lossos, A Bargal, R Sury, V Carmi, R Leitersdorf, E Zeigler, M

Citation: V. Meiner et al., Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C, GENET MED, 3(5), 2001, pp. 343-348

Authors: Sagi, M Meiner, V Reshef, N Dagan, J Zlotogora, J

Citation: M. Sagi et al., Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for highrates of pregnancy termination, PRENAT DIAG, 21(6), 2001, pp. 461-465

Authors: Ben-Dov, IZ Meiner, V Eid, A

Citation: Iz. Ben-dov et al., Kidney transplantation unraveling Wolfram syndrome: A case report, TRANSPLANT, 72(5), 2001, pp. 958-960

Authors: Durst, R Colombo, R Shpitzen, S Ben Avi, L Friedlander, Y Wexler, R Raal, FJ Marais, DA Defesche, JC Mandelshtam, MY Kotze, MJ Leitersdorf, E Meiner, V

Citation: R. Durst et al., Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: Positive selection is not always necessary to account for disease incidence among Ashkenazi Jews, AM J HU GEN, 68(5), 2001, pp. 1172-1188

Authors: Reshef, A Brauner, P Shpitzen, M Gallili, N Marbach, A Motro, U Shmueli, E Meiner, V

Citation: A. Reshef et al., Chorionic villus sampling prior to pregnancy termination, a tool for forensic paternity testing, J FOREN SCI, 44(5), 1999, pp. 1065-1068

Authors: Lossos, A Meiner, Z Barash, V Soffer, D Schlesinger, I Abramsky, O Argov, Z Shpitzen, S Meiner, V

Citation: A. Lossos et al., Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr(329)Ser mutation in the glycogen-branching enzyme gene, ANN NEUROL, 44(6), 1998, pp. 867-872