Use of in Situ Hybridization in Clinical Cytogenetics
- 1 January 1991
- journal article
- review article
- Published by Taylor & Francis in Pediatric Pathology
- Vol. 11 (4) , 497-505
- https://doi.org/10.3109/15513819109064786
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308Clinical Genetics, 2008
- High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid ClonesScience, 1990
- Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probesHuman Genetics, 1988
- Prenatal diagnosis with biotinylated chromosome specific probesPrenatal Diagnosis, 1988
- RAPID PRENATAL DIAGNOSIS OF DOWN'S SYNDROME WITH IN-SITU HYBRIDISATION OF FLUORESCENT DNA PROBESThe Lancet, 1986
- Chromosome-specific subfamilies within human alphoid repetitive DNAJournal of Molecular Biology, 1986
- Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21Cytogenetic and Genome Research, 1986
- In situ hybridization and translocation breakpoint mappingCytogenetic and Genome Research, 1984
- Unscheduled DNA synthesis after partial UV irradiation of the cell nucleusExperimental Cell Research, 1979
- New Giemsa method for the differential staining of sister chromatidsNature, 1974