Flickinger C. In search of red blood cells for alloimmunized patients with sickle cell disease. Immunohematol 2006;22:136-42.10.21307/immunohematology-2019-371Search in Google Scholar
Noizat-Pirenne F, Lee K, Pennec PY, et al. Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety. Blood 2002;100:4223-31.10.1182/blood-2002-01-022912393640Search in Google Scholar
Reid ME, Storry JR, Issitt PD, et al. Rh haplotypes that make e but not hrB usually make VS. Vox Sang 1997;72:41-4.10.1159/000461956Search in Google Scholar
Storry JR, Reid ME, Fetics S, Huang C. Mutations in the GYPB exon 5 drive the S–s–U+var phenotype in persons of African descent: implications for transfusion. Transfusion 2003;43:1738-47.10.1046/j.0041-1132.2003.00585.x14641872Search in Google Scholar
Westhoff CM. The Rh blood group system in review: a new face for the next decade. Transfusion 2004;44:1663-73.10.1111/j.0041-1132.2004.04237.x15504174Search in Google Scholar
Reid ME, Lomas-Francis C. The blood group antigen factsbook. 2nd ed. San Diego: Academic Press; 2004.10.1016/B978-012586585-2/50007-XSearch in Google Scholar
Wagner FF, Flegel WA. The Rhesus Site at http://www.uni-ulm.de/~fwagner/RH/RB/ weakD.htm.Search in Google Scholar
Blumenfeld OO, Patnaik SK. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database. Hum Mutat 2004; 23:8-16.10.1002/humu.1029614695527Search in Google Scholar
Westhoff CM, Silberstein LE, Wylie DE, Reid ME. 16Cys encoded by the RHce gene is associated with altered expression of the e antigen and is frequent in the Ro haplotype. Br J Haematol 2001;113.10.1046/j.1365-2141.2001.02803.x11380456Search in Google Scholar
Westhoff CM. Review: the Rh blood group D antigen... dominant, diverse, and difficult. Immunohematol 2005;21:155-63.10.21307/immunohematology-2019-412Search in Google Scholar
Wagner FF, Frohmajer A, Flegel WA. RHD positive haplotypes in D negative Europeans. BMC Genet 2001;2:10.10.1186/1471-2156-2-103726711495631Search in Google Scholar
Singleton BK, Green CA, Avent ND, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype. Blood 2000;95:12-8.10.1182/blood.V95.1.12Search in Google Scholar
Chiu RW, Murphy MF, Fidler C, et al. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem 2001;47:667-72.10.1093/clinchem/47.4.667Search in Google Scholar
Faas BHW, Beckers EAM, Wildoer P, et al. Molecular backgound of VS and weak C expression in blacks. Transfusion 1997;37:38-44.10.1046/j.1537-2995.1997.37197176949.x9024488Search in Google Scholar
Hemker MB, Ligthart PC, Berger L, et al. DAR, a new RhD variant involving exons 4, 5, and 7, often in linkage with ceAR, a new Rhce variant frequently found in African Blacks. Blood 1999;94:4337-42.10.1182/blood.V94.12.4337Search in Google Scholar
Lee MT, Piomelli S, Granger S, et al. Stroke Prevention Trial in Sickle Cell Anemia (STOP): Extended Follow-up and Final Results. Blood 2006.10.1182/blood-2005-10-009506189584816861341Search in Google Scholar
Adams RJ, Brambilla DJ, Granger S, et al. Stroke and conversion to high risk in children screened with transcranial Doppler ultrasound during the STOP study. Blood 2004;103:3689-94.10.1182/blood-2003-08-273314751925Search in Google Scholar