Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR)

Author:

Buchovecky Christie M.,Nahum Odelia,Levy Brynn

Publisher

Springer New York

Reference9 articles.

1. Hsu LY (1992) Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In: Milunsky A (ed) Genetic disorders and the fetus: diagnosis, prevention and treatment, 3rd edn. Johns Hopkins University Press, Baltimore

2. Ledbetter DH, Zachary JM, Simpson JL et al (1992) Cytogenetic results from the U.S. collaborative study on CVS. Prenat Diagn 12(5):317–345

3. Ledbetter DH (1993) Prenatal cytogenetics: indications, accuracy and future directions. In: Simpson JL, Elias S (eds) Essentials of prenatal diagnosis. Churchill Livingstone, New York

4. Saura R, Roux D, Taine L et al (1994) Early amniocentesis versus chorionic villus sampling for fetal karyotyping. Lancet 344(8925):825–826

5. Weida J, Patil AS, Schubert FP et al (2017) Prevalence of maternal cell contamination in amniotic fluid samples. J Matern Fetal Neonatal Med 30(17):2133–2137. https://doi.org/10.1080/14767058.2016.1240162

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