Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping
- 20 January 2005
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 25 (1), 79-83
- https://doi.org/10.1002/pd.1089
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysisPrenatal Diagnosis, 2005
- Development and targeted application of a rapid QF‐PCR test for sex chromosome imbalancePrenatal Diagnosis, 2003
- Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCRPrenatal Diagnosis, 2002
- Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosisThe Lancet, 2001
- A large‐scale evaluation of amnio‐PCR for the rapid prenatal diagnosis of fetal trisomyUltrasound in Obstetrics & Gynecology, 2001
- Maternal cell contamination in amniotic fluid samples as a consequence of the sampling techniqueHuman Genetics, 1994
- Prenatal diagnosis by in situ hybridization on uncultured amniocytes: Reduced sensitivity and potential risk of misdiagnosis in blood‐stained samplesPrenatal Diagnosis, 1993
- Cytogenetic results of chorionic villus sampling: High success rate and diagnostic accuracy in the United States collaborative studyAmerican Journal of Obstetrics and Gynecology, 1990
- European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell culturesPrenatal Diagnosis, 1984
- Maternal cell contamination of amniotic fluid cell cultures: Results of a U.S. nationwide surveyAmerican Journal of Medical Genetics, 1983