Detection of fetal cells with 47,XY,+21 karyotype in maternal peripheral blood
- 1 December 1992
- journal article
- case report
- Published by Springer Science and Business Media LLC in Human Genetics
- Vol. 90 (4), 368-370
- https://doi.org/10.1007/bf00220460
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH).1992
- Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometryAmerican Journal of Obstetrics and Gynecology, 1991
- Localizing DNA and RNA within nuclei and chromosomes by fluorescence in situ hybridizationGenetic Analysis: Biomolecular Engineering, 1991
- Prenatal sonographic findings of Down syndrome: review of 94 cases.1990
- Isolation of fetal DNA from nucleated erythrocytes in maternal blood.Proceedings of the National Academy of Sciences, 1990
- 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
- Sonographic Identification of Second-Trimester Fetuses with Down's SyndromeNew England Journal of Medicine, 1987
- Direct hybridization to DNA from small numbers of flow-sorted nucleated newborn cellsCytometry, 1987
- Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting.Proceedings of the National Academy of Sciences, 1979