Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing
- 14 August 1993
- journal article
- case report
- Published by Elsevier in The Lancet
- Vol. 342 (8868) , 403-404
- https://doi.org/10.1016/0140-6736(93)92816-c
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Breaking the blood barrierNature Genetics, 1992
- Non‐invasive first trimester antenatal diagnosisBJOG: An International Journal of Obstetrics and Gynaecology, 1992
- Detection of fetal DNA in trans‐cervical swabs from first trimester pregnancies by gene amplification: a new route to prenatal diagnosis?BJOG: An International Journal of Obstetrics and Gynaecology, 1992
- Fast one-step procedure for the detection of nucleic acids in situ by primer-induced sequence-specific labeling with fluorescein-12-dUTPCytogenetic and Genome Research, 1992
- Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84Human Genetics, 1986
- Use of the Y Chromosome in Prenatal Sex DeterminationNature, 1971