Daniels GL, Cartron JP, Fletcher A, et al. International Society of Blood Transfusion Committee on terminology for red cell surface antigens: Vancouver Report. Vox Sang 2OO3;84: 244-7.10.1046/j.1423-0410.2003.00282.xSearch in Google Scholar
Scott M. Rh serology—coordinator’s report. Transfus Clin Biol 1996;3:333-7.10.1016/S1246-7820(96)80040-1Search in Google Scholar
Scott M. Section 1A: Rh serology. Coordinator’s report.Transfus Clin Biol 2002;9:23-9.Search in Google Scholar
Tippett P, Sanger R. Observations on subdivisions of the Rh antigen D.Vox Sang 1962;7:9-13.10.1111/j.1423-0410.1962.tb03223.x13921349Search in Google Scholar
Le van Kim C, Mouro I, Cherif-Zahar B, et al. Molecular cloning and primary structure of the human blood group RhD polypeptide. Proc Nad Acad Sci USA l992;89:10925-9.10.1073/pnas.89.22.10925504551438298Search in Google Scholar
Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA, Lublin DM. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. Blood l993;82: 651-655.10.1182/blood.V82.2.651.651Search in Google Scholar
Cherif-Zahar B, Bloy C, Le Van Kim C, et al. Molecular cloning and protein structure of a human blood group Rh polypeptide. Proc Natl Acad Sci USA 1990;87:6243-7.10.1073/pnas.87.16.6243545091696722Search in Google Scholar
Avent ND, Ridgwell K, Tanner MJ, Anstee DJ. cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus>blood-group-antigen expression. Biochem J 1990;271:821-5.10.1042/bj271082111496382123099Search in Google Scholar
Wagner FĘ Gassner C, Müller TH, Schönitzer D, Schunter Ę Flegel WA. Molecular basis of weak D phenotypes. Blood 1999;93:385-93.10.1182/blood.V93.1.385Search in Google Scholar
Ridgwell K, Spurr NK, Laguda B, MacGeoch C, Avent ND, Tanner MJ. Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood- group antigen expression. Biochem J l992;287: 223-8.10.1042/bj287022311331471417776Search in Google Scholar
Nicolas V, Le Van Kim C, Gane P, et al. Rh- RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null>associated mutation. J Biol Chem 2003;278:25526-33.10.1074/jbc.M30281620012719424Search in Google Scholar
Cherif-Zahar B, Raynal V Gane P, et al. Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deflciency. Nat Genet 1996;12:168-73.10.1038/ng0296-168Search in Google Scholar
Marini AM, Matassi G, Raynal V Andre B, Cartron JP, Cherif-Zahar B.The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast. Nat Genet 2000;26:341-4.10.1038/81656Search in Google Scholar
Westhoff CM, Ferreri-Jacobia M, Mak DO, Foskett JK. Identification of the erythrocyte Rh blood group glycoprotein as a mammalian ammonium transporter. J Biol Chem 2OO2;277:12499-502.10.1074/jbc.C200060200Search in Google Scholar
Hemker MB, Cheroutre G, van Zwieten R, et al.The Rh complex exports ammonium from human red blood cells. Br J Haematol 2003;122:333-40.10.1046/j.1365-2141.2003.04425.xSearch in Google Scholar
Soupene E, King N, Feild E, et al. Rhesus expression in a green alga is regulated by CO(2). Proc Natl Acad Sci USA 2002;99:7769-73.10.1073/pnas.112225599Search in Google Scholar
Cherif-Zahar B, Le Van Kim C, Rouillac C, Raynal Y Cartron JP, Colin Y. Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region. Genomics 1994;19:68-74.10.1006/geno.1994.1014Search in Google Scholar
Wagner FĘ Flegel WA.Æffl? gene deletion occurred in the Rhesus box. Blood 2000;95:3662-8.10.1182/blood.V95.12.3662Search in Google Scholar
Suto Y, Ishikawa Y, Hyodo H, Uchikawa M, Juji T. Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber- FISH analysis. Hum Genet 2000;106:164-71.10.1007/s004390000237Search in Google Scholar
Wagner FĘ Flegel WA. RHCE represents the ancestral RH position, while RHD is the duplicated gene. Blood 2002;99:2272-3.10.1182/blood-2001-12-0153Search in Google Scholar
Kumada M, Iwamoto S, Kamesaki T, Okuda H, Kajii E. Entire sequence of a mouse chromosomal segment containing the gene Rhced and a comparative analysis of the homologous human sequence. Gene 2002;299:165-72.10.1016/S0378-1119(02)01054-5Search in Google Scholar
Colin Y, Cherif-Zahar B, Le Van Kim C, Raynal V,Van Huffel V, Cartron JP. Genetic basis of the RhD- positive and RhD-negative blood group polymorphism as determined by Southern analysis. Blood 1991;78:2747-52.10.1182/blood.V78.10.2747.2747Search in Google Scholar
Chiu RW, Murphy MF, Fidler C, Zee BC,Wainscoat JS, Lo YM. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem 2OOl;47: 667-72.10.1093/clinchem/47.4.667Search in Google Scholar
Matheson KA, Denomme GA. Novel 3’Rhesus box sequences confound RHD zygosity assignment. Transfusion 2002;42:645-50.10.1046/j.1537-2995.2002.00078.x12084174Search in Google Scholar
Wagner FĘ Moulds JM,Tounkara A, Kouriba B, Flegel WA. RHD allele distribution in Africans of Mali. BMC Genet 2OO3;4:l4.Search in Google Scholar
Wagner FĘ Frohmajer A, Flegel WA. RHD positive haplotypes in D negative Europeans. BMC Genet 2OOl;2:lO.Search in Google Scholar
Huang CH. Alteration of RH gene structure and expression in human dCCee and DCW- red blood cells: phenotypic homozygosity versus genotypic heterozygosity. Blood 1996;88:2326-33.10.1182/blood.V88.6.2326.bloodjournal8862326Search in Google Scholar
Kashiwase K, Ishikawa Y, Hyodo H, et al. E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop.Transfusion 2001;41:1408-12.10.1046/j.1537-2995.2001.41111408.x11724987Search in Google Scholar
Cheng GJ, Chen Y, Reid ME, Huang CH. Evans antigen: a new hybrid structure occurring on background of Doo and D— Rh complexes. Vox Sang 2000;78:44-51.10.1046/j.1423-0410.2000.7810044.xSearch in Google Scholar
Lomas C, Tippett P, Thompson KM, Melamed MD, Hughes-Jones NC. Demonstration of seven epitopes on the Rh antigen D using human monoclonal anti- D antibodies and red cells from D categories. Vox Sang 1989;57:261-4.10.1111/j.1423-0410.1989.tb00839.x2482582Search in Google Scholar
Beckers EAM, Faas BHW von dem Borne AEGK, Overbeeke MAM, van Rhenen DJ, van der Schoot CE. The RoHaI Rh:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene. Br J Haematol 1996;92:751-7.10.1046/j.1365-2141.1996.382918.x8616049Search in Google Scholar
Wagner FĘ Ladewig B, Flegel WA. The RHCE allele ceRT: D epitope 6 expression does not require D- specific amino acids.Transfusion 2003;43:1248-54.10.1046/j.1537-2995.2003.00495.x12919427Search in Google Scholar
Liu W, Avent ND, Jones JW Scott ML, Voak D. Molecular configuration of Rh D epitopes as defined by site-directed mutagenesis and expression of mutant Rh constructs in K562 erythroleukemia cells. Blood 1999;94:3986-96.10.1182/blood.V94.12.3986Search in Google Scholar
Wagner FĘ Flegel WA. Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles.Transfusion 1997;37:284-90.10.1046/j.1537-2995.1997.37397240210.x9122901Search 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- blood group phenotype. Blood 2000;95:12-8.10.1182/blood.V95.1.12Search in Google Scholar
Shao CP, Maas JH, Su YQ, Kohler M, Legler TJ. Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese. Vox Sang 2002;83:156-61.10.1046/j.1423-0410.2002.00192.x12201845Search in Google Scholar
Faas BH, Beckers EA, Wildoer P, et al. Molecular background ofVS and weak C expression in blacks. Transfusion 1997;37:38-44.10.1046/j.1537-2995.1997.37197176949.x9024488Search in Google Scholar
Blunt T, Daniels G, Carritt B. Serotype switching in a partially deleted RHD gene. Vox Sang l994;67:397- 401.10.1159/000462645Search in Google Scholar
Wagner FĘ Ernst M, Sonneborn HH, Flegel WA. A D(V>like phenotype is obliterated by A226P in the partial D DBS. Transfusion 2001;41:1052-8.10.1046/j.1537-2995.2001.41081052.x11493738Search in Google Scholar
Wagner FĘ Gassner C, Müller TH, Schönitzer D, Schunter Ę Flegel WA. Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features. Blood 1998;91:2157-68.10.1182/blood.V91.6.2157Search in Google Scholar
Omi T, Okuda H, Iwamoto S, et al. Detection of Rh23 in the partial D phenotype associated with the D(Va) category.Transfusion 2000;40:256-8.10.1046/j.1537-2995.2000.40020256.x10686014Search in Google Scholar
Mouro I, Le Van Kim C, Rouillac C, et al. Rearrangements of the blood group RhD gene associated with the DVI category phenotype. Blood 1994;83:1129-35.10.1182/blood.V83.4.1129.1129Search in Google Scholar
Rouillac C, Colin Y, Hughes-Jones NC, et al. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. Blood 1995;85:2937-44.10.1182/blood.V85.10.2937.bloodjournal85102937Search in Google Scholar
Beckers EA, Faas BH, Simsek S, et al. The genetic basis of a new partial D antigen: DDBT. Br J Haematol 1996;93:720-7.10.1046/j.1365-2141.1996.d01-1710.x8652401Search in Google Scholar
Lomas C, Grassmann W, Ford D, et al. FPTT is a low- incidence Rh antigen associated with a “new” partial Rh D phenotype, DFR. Transfusion 1994;34:612-6.10.1046/j.1537-2995.1994.34794330017.x7519797Search in Google Scholar
Tippett P, Lomas-Francis C, Wallace M. The Rh antigen D: partial D antigens and associated low incidence antigens.Vox Sang l996;7O(3):l23-3l.Search in Google Scholar
Rouillac C, Le Van Kim C, Blancher A, Roubinet Ę Cartron JP, Colin Y. Lack of G blood group antigen in DΠIb erythrocytes is associated with segmental DNA exchange between RH genes. Br J Haematol 1995;89:424-6.10.1111/j.1365-2141.1995.tb03323.x7873397Search in Google Scholar
Beckers EA, Faas BH, Ligthart P, et al. Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotype. Transfusion 1996;36:567-74.10.1046/j.1537-2995.1996.36696269518.x8669091Search in Google Scholar
Flegel WA. Rhesus Immunisierungsregister (RIR) [The Rhesus Immunization Surveillance]. Ulm: DRK Blutspendedienst Baden-Württemberg-Hessen. http://www.uni-ulm.de/~wflegel/RH/RIR/>.Search in Google Scholar
Wagner FĘ Eicher NI, Jorgensen JR, Lonicer CB, Flegel WA. DNB: a partial D with anti-D frequent in Central Europe. Blood 2002;100:2253-6.10.1182/blood-2002-03-074212200394Search in Google Scholar
Rouillac C, Le Van Kim C, Beolet M, Cartron JP, Colin Y LeullOPro substitution in the RhD polypeptide is responsible for the DVΠ category blood group phenotype. Am J Hematol 1995;49:87-8.10.1002/ajh.28304901157741145Search in Google Scholar
Wagner FĘ Frohmajer A, Ladewig B, et al. Weak D alleles express distinct phenotypes. Blood 2000;95:2699-708.10.1182/blood.V95.8.2699Search in Google Scholar
Müller TH, Wagner FĘ Trockenbacher A, et al. PCR screening for common weak D types shows different distributions in three Central European populations.Transfusion 2001 ;4l:45-52.10.1046/j.1537-2995.2001.41010045.x11161244Search in Google Scholar
Cowley NM, Saul A, Hyland CA. RHD gene mutations and the weak D phenotype: an Australian blood donor study.Vox Sang 2000;79:251-2.10.1046/j.1423-0410.2000.7940252.xSearch in Google Scholar
Döscher A, Ladewig B, Das Gupta C, et al. Molecular genetic RHD characterization of 577 cases with serologic suspect for weak D (abstract). Transfus Med Hemother 2OO3;3OSl:B2.O3.Search in Google Scholar
Kamesaki T, Iwamoto S, Kumada M, et al. Molecular characterization of weak D phenotypes by site- directed mutagenesis and expression of mutant Rh- green fluorescence protein fusions in K562 cells. Vox Sang 2001;81:254-8.10.1046/j.1423-0410.2001.00118.x11904002Search in Google Scholar
Wagner FF. Die molekulare Basis der RH- Haplotypen mit schwacher Expression des Antigens D [The molecular basis of RH haplotypes expressing weak D antigens], Habilitationsschrift. Universität Ulm; 1999. http://vts.uni-ulm.de/query/longview.meta.asp?document_id=584>Search in Google Scholar
Huang CH, Chen Y, Reid M. Human D(IIIa) erythrocytes: RhD protein is associated with multiple dispersed amino acid variations. Am J Hematol l997;55:139-45.10.1002/(SICI)1096-8652(199707)55:3<139::AID-AJH4>3.0.CO;2-TSearch in Google Scholar
Hemker MB, Ligthart PC, Berger L, van Rhenen DJ, van der Schoot CE,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;94:4337-42.10.1182/blood.V94.12.4337Search in Google Scholar
Wagner FĘ Ladewig B, Angert KS, Heymann GA, Eicher NI, Flegel WA. The DAU allele cluster of the RHD gene. Blood 2002; 100:306-11.10.1182/blood-2002-01-0320Search in Google Scholar
Mouro I, Colin Y, Cherif-Zahar B, Cartron JP, Le Van Kim C. Molecular genetic basis of the human Rhesus blood group system. Nat Genet 1993;5:62-5.10.1038/ng0993-62Search in Google Scholar
Faas BH, Beuling EA, Ligthart PC, van Rhenen DJ, van der Schoot CE. Partial expression of RHc on the RHD polypeptide.Transfusion 2001;41:1136-42.10.1046/j.1537-2995.2001.41091136.xSearch in Google Scholar
Faas BH, Beckers EA, Simsek S, et al. Involvement of Seri 03 of the Rh polypeptides in G epitope formation. Transfusion 1996;36:506-11.10.1046/j.1537-2995.1996.36696269508.xSearch in Google Scholar
Hundhausen T, Petershofen EK, Doescher A, Bauerfeind U, Muller TH, Schunter F. RHCE-D-CE hybrid genes can cause false-negative DNA typing of the Rh e antigen. Vox Sang 2002 Oct;83(3):268- 72.10.1046/j.1423-0410.2002.00220.xSearch in Google Scholar
Carritt B, Kemp TJ, Poulter M. Evolution of the human RH (rhesus) blood group genes: a 50 year old prediction (partially) fulfilled. Hum Mol Genet 1997 Jun;6(6):843-50.10.1093/hmg/6.6.843Search in Google Scholar
Poulter M, Kemp TJ, Carritt B. DNA-based Rhesus typing: simultaneous determination of RHC and RHD status using the polymerase chain reaction. Vox Sang 1996;7:164-8.10.1111/j.1423-0410.1996.tb01316.xSearch in Google Scholar
Mouro I, Colin Y, Gane P, et al. Molecular analysis of blood group Rh transcripts from a rGr variant. Br J Haematol 1996;93:472-4.10.1046/j.1365-2141.1996.4851028.xSearch in Google Scholar
Wolter LC, Hyland CA, Saul A. Refining the DNA polymorphisms that associate with the rhesus c phenotype. Blood 1994;84:985-6.10.1182/blood.V84.3.985.985Search in Google Scholar
Gassner C, Schmarda A, Kilga-Nogler S, et al. RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion 1997; 37:1020-6.10.1046/j.1537-2995.1997.371098016439.x9354819Search in Google Scholar
Daniels GL, Faas BH, Green CA, et al. The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis.Transfusion 1998;38:951-8.10.1046/j.1537-2995.1998.381098440860.x9767746Search in Google Scholar
Avent ND, Reid ME. The Rh blood group system: a review. Blood 2000;95:375-87.10.1182/blood.V95.2.375Search in Google Scholar
Blumenfeld OO, Reid ME, Huang CH. Blood group antigen gene mutation database: rare alleles of RH loci. New York, accessed 2003: http://www.bioc.aecom.yu.edu/bgmut/rh_rare.htm>Search in Google Scholar
Huang CH, Reid ME, Chen Y. Identification of a partial internal deletion in the RH locus causing the human erythrocyte D— phenotype. Blood 1995; 86:784-90.10.1182/blood.V86.2.784.bloodjournal862784Search in Google Scholar
Cherif-Zahar B, Raynal V Cartron JP. Lack of RHCE- encoded proteins in the D- -phenotype may result from homologous recombination between the two RH genes. Blood 1996;88:1518-20.10.1182/blood.V88.4.1518.bloodjournal8841518Search in Google Scholar
Huang CH, Chen Y, Reid M, Ghosh S. Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene. Am J Hum Genet 1996;59:825-33.Search in Google Scholar
Cotorruelo CM, Biondi CS, Borras SE, Di Monaco RA, Racca A. A De- phenotype encoded by an RHCE-D(5-7/8)-CE hybrid allele. Vox Sang 2003; 85:102-8.10.1046/j.1423-0410.2003.00332.x12925162Search in Google Scholar
Cherif-Zahar B, Raynal Y D’Ambrosio AM, Cartron JP, Colin Y. Molecular analysis of the structure and expression of the RH locus in individuals with D--, Dc-, and DCw- gene complexes. Blood 1994;84:4354-60.10.1182/blood.V84.12.4354.bloodjournal84124354Search in Google Scholar
Noizat-Pirenne Ę 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
Huang CH, Chen Y, Reid ME, Seidl C. Rh⊓^ disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background. Blood 1998;92:664-71.10.1182/blood.V92.2.664Search in Google Scholar
Cherif-Zahar B, Matassi G, Raynal V et al. Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type. Blood 1998;92:639-46.10.1182/blood.V92.2.639Search in Google Scholar
Avent ND, Poole J, Singleton B, et al. Studies of two partial Ds: DMH and DOL (abstract). Transfus Med 9, l999;33(suppl):33.Search in Google Scholar
Wagner FĘ Gassner C, Eicher NI, Lonicer C, Flegel WA. Characterization of D category ΓV type iγ DFW, and DNB (abstract). Transfusion 1998; 38(suppl): 63s.Search in Google Scholar
Jones JW, Finning K, Mattock R, et al.The serological profile and molecular basis of a new partial D phenotype, DHR.Vox Sang 1997;73:252-6.10.1159/000461941Search in Google Scholar
Liu W, Jones JW, Scott ML, Voak D, Avent ND. Molecular analysis of two D-variants, DHMi and DHMii (abstract). Transfus Med 6 1996; 21(suppl):21.Search in Google Scholar
Döscher A, Ladewig B, Gerdes I, et al. Six new RHD- alleles with previously unknown polymorphisms (abstract). Transfus Med Hemother 2OO3;3O(suppl 1):B2.04.Search in Google Scholar
Avent ND, Jones JW, Liu W, et al. Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3,4 and 9 to the sixth external domain of the Rh D protein. Br J Haematol 1997;97:366-71.10.1046/j.1365-2141.1997.632710.x9163603Search in Google Scholar
Körmöczi GĘ Legler TJ, Daniels GL, et al. A novel partial RhD with highly retained epitope composition in an individual with alloanti-D (abstract). Transfus Med Hemother 2OO3;3O(suppl 1):B2.07.Search in Google Scholar
Witter B. Die Verteilung von Antigendichten und weak D-Allelen im Rhesusphänotyp ccD.Ee Dissertationsschrift. Universität Ulm; 2000. http://vts.uni-ulm.de/query/longview.meta.asp?document_id=7ó5>Search in Google Scholar
Noizat-Pirenne Ę Mouro I, Gane P, et al. Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript. Br J Haematol 1998;103:429-36.10.1046/j.1365-2141.1998.01004.x9827916Search in Google Scholar
Rouillac C, Gane P, Cartron J, Le Pennec PY, Cartron JP, Colin Y. Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in Rh phenotypes. Blood 1996;87:4853-61.10.1182/blood.V87.11.4853.bloodjournal87114853Search in Google Scholar
Noizat-Pirenne F, Le Pennec PY, Mouro I, et al. Molecular background of D(C)(e) haplotypes within the white population. Transfusion 2OO2;42: 627-33.10.1046/j.1537-2995.2002.00097.x12084172Search in Google Scholar
Mouro I, Colin Y, Sistonen P, Le Pennec PY, Cartron JP, Le Van Kim C. Molecular basis of the RhCw (Rh8) and RhCx (Rh9) blood group specificities. Blood 1995;86:1196-201.10.1182/blood.V86.3.1196.1196Search in Google Scholar
Faas BH, Ligthart PC, Lomas-Francis C, Overbeeke MA, von dem Borne AE, van der Schoot CE. Involvement of Gly96 in the formation of the Rh26 epitope.Transfusion l997;37:1123-30.10.1046/j.1537-2995.1997.37111298088040.x9426634Search in Google Scholar
Westhoff CM, Silberstein LE,Wylie DE, Skavdahl M, Reid ME. l6Cys 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;113:666-71.10.1046/j.1365-2141.2001.02803.x11380456Search in Google Scholar
Huang CH, Reid ME, Chen Y, Novaretti M. Deletion of Arg 229 in RhCE polypeptide alters expression of Rhe and ce-associated Rh6 antigen (abstract). Blood l992;9O(suppl):272a.Search in Google Scholar
Noizat-Pirenne Ę Mouro I, Le Pennec PY, et al. Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI. Br J Haematol 2001;113:672-9.10.1046/j.1365-2141.2001.02802.x11380457Search in Google Scholar
Schlanser G, Moulds MK, Flegel WA, Wagner FĘ Frame T. Crawford (Rh43), a low-incidence antigen, is associated with a novel RHCE variant RHce allele, ceCF (abstract). Transfusion 2OO3;43(suppl): 35A.Search in Google Scholar
