Figure 4
Figure 4. Fluorescent in situ hybridization (FISH) of chromosome 3q26 and 3q21 loci reveal hidden 3q26 aberrations. BAC clone localization from centromere (Cen) to telomere (Tel) (A). A metaphase from EVI1+ patient no. 28 revealed a cryptic inv(3)(q21q26) (inv3) and a normal chromosome 3 (nor3) using EVI1 (RP11-82C9) and MDS1 (RP11-141C22) (B) and RPN1 (RP11-456K4) BAC clones (C). Micrographs after FISH were acquired by imaging with a fluorescence microscope (Axio-Imager Z1; Zeiss, Sliedrecht, The Netherlands) fitted with a Plan-Apochromat at 100x/1.40 numeric aperture oil objective, a CCD video camera (Metasystems, Altlussheim, Germany), and using Isis software for capturing and processing fluorescent images (v5.1.7, Metasystems).

Fluorescent in situ hybridization (FISH) of chromosome 3q26 and 3q21 loci reveal hidden 3q26 aberrations. BAC clone localization from centromere (Cen) to telomere (Tel) (A). A metaphase from EVI1+ patient no. 28 revealed a cryptic inv(3)(q21q26) (inv3) and a normal chromosome 3 (nor3) using EVI1 (RP11-82C9) and MDS1 (RP11-141C22) (B) and RPN1 (RP11-456K4) BAC clones (C). Micrographs after FISH were acquired by imaging with a fluorescence microscope (Axio-Imager Z1; Zeiss, Sliedrecht, The Netherlands) fitted with a Plan-Apochromat at 100x/1.40 numeric aperture oil objective, a CCD video camera (Metasystems, Altlussheim, Germany), and using Isis software for capturing and processing fluorescent images (v5.1.7, Metasystems).

Close Modal

or Create an Account

Close Modal
Close Modal