Schneider et al., 1995
ViewPDF| Publication | Publication Date | Title | 
|---|---|---|
| Schneider et al. | Loss of chromosomes 22 and 14 in the malignant progression of meningiomas: A comparative study of fluorescence in situ hybridization (FISH) and standard cytogenetic analysis | |
| Meltzer et al. | Rapid generation of region specific probes by chromosome microdissection and their application | |
| Konopleva et al. | The anti‐apoptotic genes Bcl‐XL and Bcl‐2 are over‐expressed and contribute to chemoresistance of non‐proliferating leukaemic CD34+ cells | |
| Schwartz et al. | p53 controls low DNA damage-dependent premeiotic checkpoint and facilitates DNA repair during spermatogenesis | |
| Maguer-Satta et al. | BCR-ABL expression in different subpopulations of functionally characterized Ph+ CD34+ cells from patients with chronic myeloid leukemia | |
| Coonen et al. | Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa | |
| Qian et al. | Chromosomal anomalies in atypical adenomatous hyperplasia and carcinoma of the prostate using fluorescence in situ hybridization | |
| Schwartz et al. | Selective elimination of human lymphoid cells with unstable chromosome aberrations by p53-dependent apoptosis. | |
| Wernicke et al. | Involvement of chromosome 22 in ependymomas | |
| Desmaze et al. | Unicolor and bicolor in situ hybridization in the diagnosis of peripheral neuroepithelioma and related tumors | |
| Taylor et al. | Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridisation on tumour imprints and bone marrow smears | |
| Gardiner et al. | Cytogenetic, fluorescence in situ hybridisation, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukaemia | |
| Reid et al. | bcl-2 rearrangement in Hodgkin's disease. Results of polymerase chain reaction, flow cytometry, and sequencing on formalin-fixed, paraffin-embedded tissue | |
| Kobayashi et al. | Analysis of chromosome 17p13 (p53 locus) alterations in gastric carcinoma cells by dual-color fluorescence in situ hybridization | |
| Morel et al. | Meiotic segregation of at (7; 8)(q11. 21; cen) translocation in two carrier brothers | |
| Acar et al. | Micronucleus incidence and their chromosomal origin related to therapy in acute lymphoblastic leukemia (ALL) patients: detection by micronucleus and FISH techniques | |
| M'kacher et al. | Baseline and treatment-induced chromosomal abnormalities in peripheral blood lymphocytes of Hodgkin's lymphoma patients | |
| Choi-Hong et al. | Twin pregnancies with complete hydatidiform mole and coexisting fetus: use of fluorescent in situ hybridization to evaluate placental X-and Y-chromosomal content | |
| Sotomayor et al. | In situ follicular lymphoma with a 14; 18 translocation diagnosed by a multimodal approach | |
| Umeki et al. | Flow cytometric measurements of somatic cell mutations in Thorotrast patients | |
| Wyrobek et al. | Chromosomally defective sperm and their developmental consequences | |
| Balazs et al. | Karyotypic heterogeneity and its relation to labeling index in interphase breast tumor cells | |
| Karda et al. | Translocation (X; 1)(p11. 2; q21) in a papillary renal cell carcinoma in a 14-year-old girl | |
| Wojcik | Comparison of radiation-induced aberration frequencies in chromosomes 1 and 2 of two human donors | |
| Angel et al. | Analysis of antigen receptor genes in Hodgkin's disease. |