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The prevalence of red cell antibodies in pregnancy correlated to the outcome of the newborn: A 12 year study in central Sweden
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0028875503
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Frequencies of the blood groups ABO, Rhesus, D category VI, Kell, and of clinically relevant high-frequency antigens in South-Western Germany
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Wagner FF, Kasulke D, Kerowgan M and Flegel WA: Frequencies of the blood groups ABO, Rhesus, D category VI, Kell, and of clinically relevant high-frequency antigens in South-Western Germany. Infusionsther Transfusionsmed 1995, 22:285-290.
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0032932817
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Molecular basis of weak D phenotypes
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Wagner FF, Gassner C, Müller TH, Schönitzer D, Schunter F and Flegel WA: Molecular basis of weak D phenotypes. Blood 1999, 93:385-393.
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Frequency of partial D phenotypes in the south western region of France
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Roubinet, F.1
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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
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Singleton BK, Green CA, Avent ND, Martin PG, Smart E, Daka A, Narter-Olaga EG, Hawthorne LM and Daniels G: 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, 95:12-18.
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Blood
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Molecular background of VS and weak C expression in blacks
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Faas BH, Beckers EA, Wildoer P, Ligthart PC, Overbeeke MA, Zondervan HA, von dem Borne AE and van der Schoot CE: Molecular background of VS and weak C expression in blacks. Transfusion 1997, 37:38-44.
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0032762182
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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
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Hemker MB, Ligthart PC, Berger L, van Rhenen DJ, van der Schoot CE and Wijk PA: 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, 94:4337-4342.
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Wijk, P.A.6
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9
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The DAU allele cluster of the RHD gene
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Wagner FF, Ladewig B, Angert KS, Heymann GA, Eicher NI and Flegel WA: The DAU allele cluster of the RHD gene. Blood 2002, 100:306-311.
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0034659823
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RHD gene deletion occurred in the Rhesus box
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Wagner FF and Flegel WA: RHD gene deletion occurred in the Rhesus box. Blood 2000, 95:3662-3668.
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Blood
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Novel 3′ Rhesus box sequences confound RHD zygosity assignment
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Matheson KA and Denomme GA: Novel 3′ Rhesus box sequences confound RHD zygosity assignment. Transfusion 2002, 42:645-650.
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The distribution of the human blood groups and other polymorphisms
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Mourant AE, Kopec AC and Domaniewska-Sobczak K: The distribution of the human blood groups and other polymorphisms. London: Oxford University Press 1976.
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Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype
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Rodrigues A, Rios M, Pellegrino J Jr, Costa FF and Castilho L: Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype. Braz J Med Biol Res 2002, 35:767-773.
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The VS and V blood group polymorphisms in Africans: A serologic and molecular analysis
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Daniels GL, Faas BH, Green CA, Smart E, Maaskant-van Wijk PA, Avent ND, Zondervan HA, von dem Borne AE and van der Schoot CE: The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion 1998, 38:951-958.
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Testing for the D zygosity with three different methods revealed altered Rhesus boxes and a new weak D type
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Perco P, Shao CP, Mayr WR, Panzer S and Legler TJ: Testing for the D zygosity with three different methods revealed altered Rhesus boxes and a new weak D type. Transfusion 2003, 43:335-339.
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Weak D alleles express distinct phenotypes
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Wagner FF, Frohmajer A, Ladewig B, Eicher NI, Lonicer CB, Muller TH, Siegel MH and Flegel WA: Weak D alleles express distinct phenotypes. Blood 2000, 95:2699-2708.
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0027293541
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Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals
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Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA and Lublin DM: Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. Blood 1993, 82:651-655.
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