Noninvasive fetal RhCE genotyping from maternal blood
Author:
Publisher
Wiley
Subject
Obstetrics and Gynecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-0528.2008.01744.x/fullpdf
Reference30 articles.
1. PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease;Le Van Kim;Br J Haematol,1994
2. Rapid molecular determination of fetal rhesus E type;Geifman-Holtzman;Prenat Diagn,1996
3. Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers;Lo;Lancet,1993
4. Fetal RhD genotyping in fetal cells flow sorted from maternal blood;Geifman-Holtzman;Am J Obstet Gynecol,1996
5. Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma;Amicucci;Clin Chem,2000
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1. Confirmed non‐invasive prenatal testing for foetal Rh blood group genotyping along with bi‐allelic short insertion/deletion polymorphisms as a positive internal control;Transfusion Medicine;2022-03-09
2. Non-Invasive Prenatal Fetal Blood Group Genotype and Its Application in the Management of Hemolytic Disease of Fetus and Newborn: Systematic Review and Meta-Analysis;Transfusion Medicine Reviews;2021-04
3. Management of red blood cell alloimmunization in pregnancy;Journal of Gynecology Obstetrics and Human Reproduction;2018-05
4. High-Risk Pregnancy;2017-11-15
5. Hemolytic disease of the fetus and newborn in the molecular era;Seminars in Fetal and Neonatal Medicine;2016-02
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