An Improved Method for the Detection of Trisomy 21 in Uncultured Amniocytes by Fluorescence in Situ Hybridizationa
- 1 September 1994
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 731 (1) , 67-72
- https://doi.org/10.1111/j.1749-6632.1994.tb55749.x
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contigPrenatal Diagnosis, 1992
- Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cellsHuman Molecular Genetics, 1992
- Rapid detection of human chromosome 21 aberrations by in situ hybridization.Proceedings of the National Academy of Sciences, 1988
- Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probesHuman Genetics, 1988