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Medical and Pediatric Oncology|January 1, 1991
Lack of bcr rearrangement in juvenile chronic myeloid leukemiaA Toren, M Mandel, N Amariglio, et al.
American Journal of Human Genetics|December 1, 1999
Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13A Toren, N Amariglio, G Rozenfeld-Granot, et al.
American Journal of Hematology|February 24, 2005
Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer developmentM Koren-Michowitz, E Friedman, R Gershoni-Baruch, et al.
Cancer Genetics and Cytogenetics|February 25, 2000
Coexistence of several unbalanced translocations in a case of neuroblastoma: the contribution of multicolor spectral karyotypingL Trakhtenbrot, N Cohen, E Rosner, et al.
Bone Marrow Transplantation|May 16, 2003
B-cell lymphoma developing in the donor 9 years after donor-origin acute myeloid leukemia post bone marrow transplantationB Bielorai, H J Deeg, M Weintraub, et al.
Journal of Dental Research|January 26, 2007
P2X4 is up-regulated in gingival fibroblasts after periodontal surgeryI Binderman, H Bahar, J Jacob-Hirsch, et al.
Scandinavian Journal of Immunology|November 16, 2004
Unique TCRDV1-positive lymphocytes that infiltrate colonic neoplasia originate from a selected cell population present in the intestinal mucosa and the peripheral bloodD Coscas, M Chowers, M Levite, et al.
Bone Marrow Transplantation|June 20, 2003
Tetraploid myeloid cells in donors of peripheral blood stem cells treated with rhG-CSFC Kaplinsky, L Trakhtenbrot, I Hardan, et al.
British Journal of Cancer|July 17, 2003
Overexpression of a set of genes, including WISP-1, common to pulmonary metastases of both mouse D122 Lewis lung carcinoma and B16-F10.9 melanoma cell linesO Margalit, L Eisenbach, N Amariglio, et al.
Clinical Genetics|March 18, 2004
Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndromeU Tabori, Z Mark, N Amariglio, et al.
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