Severe erythroblastosis in a primigravida associated with absence of Rh chromosomes
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference9 articles.
1. A Probable Deletion in a Human Rh Chromosome
2. Blood Genotypes -D-/-D- and CDE/-D- Transfusion Therapy and Some Effects of Multiple Pregnancy
3. Consanguinity and Two Rare Matings.
4. Two Examples of the -D-/-D- Genotype in an American Family
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1. Recurrent pregnancy loss in a patient with anti‐Rh17;Transfusion Medicine;2023-11-08
2. Maternal red blood cell alloimmunisation Working Party, literature review. RH blood group system: Rare specificities;Transfusion Clinique et Biologique;2021-08
3. First report of the rare RhCE‐depleted D‐‐phenotype in sixteen people of Iranian origin;Vox Sanguinis;2019-02-19
4. Management of a full-term infant with hemolytic disease of the newborn due to an anti-Rh17 antibody in a mother with D-- phenotype;American Journal of Hematology;2005
5. Maternal ABO-mismatched blood for intrauterine transfusion of severe hemolytic disease of the newborn due to anti-Rh17;Transfusion;2004-08-17
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