Fluorescent in situ hybridization on archival G-banded slides

Cytogenetics and Cell Genetics

Volumn 73, Issue 4, 1996, Pages 322-324

  El Rifai, W ^a,b   Knuutila, S ^a  

^a Department of Medical Genetics ^*  (Egypt)

^b NATIONAL RESEARCH CENTRE   (Egypt)

Author keywords

[No Author keywords available]

Indexed keywords

XYLENE;

AMINO ACID SEQUENCE; ARTICLE; CELL CULTURE; CHROMOSOME ABERRATION; CHROMOSOME PAINTING; CULTURAL ANTHROPOLOGY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; MARKER CHROMOSOME; PRIORITY JOURNAL;

CHROMOSOME BANDING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOMONOCYTIC, ACUTE; LEUKEMIA, NONLYMPHOCYTIC, ACUTE; PRESERVATION, BIOLOGICAL; SPECIMEN HANDLING; TRANSLOCATION, GENETIC;

EID: 0029823991     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134367     Document Type: Article

References (5)

1. Babu VR, Wiktor A: A fluorescence in situ hybridization technique for retrospective cytogenetic analysis. Cytogenel Cell Genet 57:16-17(1991).
2. Cremer T, Lichter P, Borden J, Ward DC, Manuelidis L: Detection of chromosome aberrations in metaphase and intcrphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum Genet 80:235-246 (1988).
3. Knuutila S: Genotype and phenotype on the same interphase or mitotic cell, in Dracopoli NC, Haines JL, Korf BR, Moir DT. Morton CC. Seidman CE, Seidman JG, Smilh DR (eds): Current Protocols for Human Genetics, Unit 4.7 (Greene & Wiley. Madison, CT 1996).
4. Schad CR, Kraker WJ, Jalal SM, Tallman MS, Londer HN, Cook LP, Jenkins RB: Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disorders. Am J clin Pathol 96:203-210 (1991).
5. Tarkkanen M, Böhling T, Heliö H, Karaharju E, Kai-painen A, Szymanska J, Elomaa I, Knuutila S: A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(ql 3;p21p25) and 2p deletion: a ease report. Cancer Genet Cytogenet 65:141-146(1993).