Fluorescent in Situ Hybridization for the Diagnosis of Genetic Disease at Postnatal, Prenatal, and Preimplantation Stages
- 1 January 1994
- book chapter
- Published by Elsevier
- Vol. 153, 1-40
- https://doi.org/10.1016/s0074-7696(08)62187-7
Abstract
No abstract availableThis publication has 69 references indexed in Scilit:
- Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping, banding, and investigation of sequence organizationCytogenetic and Genome Research, 1991
- Fluorescence in situ hybridization: applications in cytogenetics and gene mappingTrends in Genetics, 1991
- Human gametes and zygotes studied by nonradioactive in situ hybridizationCytogenetic and Genome Research, 1990
- Rapid sexing of human embryos by non-radioactivein situ hybridization: Potential for preimplantation diagnosis of X-linked disordersPrenatal Diagnosis, 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
- RAPID PRENATAL DIAGNOSIS OF DOWN'S SYNDROME WITH IN-SITU HYBRIDISATION OF FLUORESCENT DNA PROBESThe Lancet, 1986
- Aminomethyl coumarin acetic acid: A new fluorescent labelling agent for proteinsJournal of Molecular Histology, 1986
- 2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequencesExperimental Cell Research, 1984
- Parental origin of autosomal trisomiesAnnals of Human Genetics, 1984