Fetal RhD genotyping: A more efficient use of anti-D immunoglobulin
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology
Reference22 articles.
1. Human Blood Groups;Daniels,2002
2. RHD gene deletion occurred in the Rhesus box;Wagner;Blood,2000
3. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in most Africans with the Rh D-negative blood group phenotype;Singleton;Blood,2000
4. Molecular background of VS and weak C expression in blacks;Faas;Transfusion,1997
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1. Prenatal RHD genotyping in Croatia: preliminary results;Transfusion Clinique et Biologique;2021-02
2. Prevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus;BMC Research Notes;2016-04-01
3. Rhesus and Other Fetomaternal Incompatibilities;Reference Module in Biomedical Sciences;2014
4. Survey on the prevention and incidence of haemolytic disease of the newborn in Italy;BLOOD TRANSFUS-ITALY;2013
5. Cost-Effectiveness of the Management of Rh-Negative Pregnant Women;Journal of Obstetrics and Gynaecology Canada;2013-08
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