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Results: 1-25 | 26-31 |
Results: 26-31/31
Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiency
Authors: Toren, A Nagler, A Amariglio, N Neumann, Y Golan, H Bilori, B Kaplinsky, C Mandel, M Biniaminov, M Levanon, M Rosenthal, E Davidson, J Brok-Simoni, F Rechavi, G
Citation: A. Toren et al., Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiency, BONE MAR TR, 23(4), 1999, pp. 405-408
Coexistence of several unbalanced translocations in a case of neuroblastoma: The contribution of multicolor spectral karyotyping
Authors: Trakhtenbrot, L Cohen, N Rosner, E Gipsh, N Brok-Simoni, F Mandel, M Amariglio, N Rechavi, G
Citation: L. Trakhtenbrot et al., Coexistence of several unbalanced translocations in a case of neuroblastoma: The contribution of multicolor spectral karyotyping, CANC GENET, 112(2), 1999, pp. 119-123
C-kit activating mutation in a neonate with in-utero presentation of systemic mastocytosis associated with myeloproliferative disorder
Authors: Kuint, J Bielorai, B Gilat, D Birenbaum, E Amariglio, N Rechavi, G
Citation: J. Kuint et al., C-kit activating mutation in a neonate with in-utero presentation of systemic mastocytosis associated with myeloproliferative disorder, BR J HAEM, 106(3), 1999, pp. 838-839
Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13
Authors: Toren, A Amariglio, N Rozenfeld-Granot, G Simon, AJ Brok-Simoni, F Pras, E Rechavi, G
Citation: A. Toren et al., Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13, AM J HU GEN, 65(6), 1999, pp. 1711-1717
Early fulminant leukaemia post autologous bone marrow transplantation in non-Hodgkin's lymphoma patients
Authors: Toren, A Rechavi, G Nagler, A
Citation: A. Toren et al., Early fulminant leukaemia post autologous bone marrow transplantation in non-Hodgkin's lymphoma patients, MED ONCOL, 15(2), 1998, pp. 109-112
An identical novel mutation in BRCA1 and a common haplotype in familial ovarian cancer in non-Ashkenazi Jews
Authors: Theodor, L Bar-Sade, R Kruglikova, A Ben-Baruch, G Risel, S Shiri-Sverdlov, R Yechezkel, GH Modan, B Papa, MZ Rechavi, G Friedman, E
Citation: L. Theodor et al., An identical novel mutation in BRCA1 and a common haplotype in familial ovarian cancer in non-Ashkenazi Jews, BR J CANC, 77(11), 1998, pp. 1880-1883
Risultati: 1-25 | 26-31 |