Severe Haemolytic Disease in an Infant Born to an RhnullProposita
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1423-0410.1992.tb01217.x/fullpdf
Reference14 articles.
1. Haematological aspect of Rh deficiency syndrome: A case report and review of the literature;Nash;Am J Hematol,1987
2. A sample of blood with no detectable Rh antigens;Vos;Lancet,1961
3. Isolation of membrane components associated with human red cell antigens Rh (D), (c), (E) and Fya;Moore;Nature,1982
4. Absence of two membrane proteins containing extracellular thiol groups in Rhnull human erythrocytes;Ridgwell;Biochem J,1983
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1. Severe fetal anaemia due to red cell alloimmunisation in a Rhnull woman: A case report;Transfusion Medicine;2023-08-10
2. Maternal red blood cell alloimmunisation Working Party, literature review. RH blood group system: Rare specificities;Transfusion Clinique et Biologique;2021-08
3. Short duplication within theRHCEgene associated with an in cis deletedRHDcausing a Rhnullamorph phenotype in an immunized pregnant woman with anti-Rh29;Transfusion;2014-11-21
4. Haemolytic Disease of the Fetus and the Newborn;Mollison's Blood Transfusion in Clinical Medicine;2013-11-30
5. Rh and RHAG Blood Group Systems;Human Blood Groups;2013-01-28
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