Clinical applications of fluorescence in situ hybridization
- 30 April 1991
- journal article
- review article
- Published by Elsevier in Genetic Analysis: Biomolecular Engineering
- Vol. 8 (2), 67-74
- https://doi.org/10.1016/1050-3862(91)90051-r
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8Nature, 1990
- Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16pCytogenetic and Genome Research, 1990
- Early dihydrofolate reductase gene amplification events in CHO cells usually occur on the same chromosome arm as the original locus.Genes & Development, 1989
- Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridizationCancer Genetics and Cytogenetics, 1989
- Labeling of human centromeres using an alphoid DNA consensus sequence: application to the scoring of chromosome aberrationsMutation Research Letters, 1989
- Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific α satellite DNA from human chromosomes 1 and 7Cytogenetic and Genome Research, 1989
- Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA librariesHuman Genetics, 1988
- Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probesHuman Genetics, 1988
- Human Chromosome–Specific DNA Libraries: Construction and AvailabilityNature Biotechnology, 1986
- Chromosomal localization of a unique gene by non-autoradiographic in situ hybridizationNature, 1985