-
-
-
[1] KOELEWIJN J M, VRIJKOTLE T G, VANDER SCHOOL C E. Effect of screening for red cell antibodies other than anti-D to detect haemolytic disease of the foetus and newborn. A postulation study in Netherlands[J].Transfusion,2009:48-941.
[2] DANIELS G. Human Blood Groups, 2nd ed[J]. Oxford'Blackwell Science;2002.
[3] WAGNER F F, MOULDS J M, FLEGEL W A. Genetic mechanisms of Rhesus box variation[J].Blood 2005,45:338-444.
[4] BURTON N M, ANSTEE D J.Structure, function and signi?cance of Rh proteins in red cells[J].Curr pin Hematol,2008,15:625-630.
[5] FAAS B H W, BECKERS E A M, WILDOER P,et al.Molecular background of VS and weak C expression in blacks[J].Transfusion,1997,37:38-44.
[6] DENOMME G A.The structure and function of the molecules that carry human red blood cell and platelet antigens[J].Transfus Med Rev,2004,18:203-31.
[7] HUANG C H, PENG J, CHEN H C,et al.RH locus contraction in a novel Dc-/D-genotype resulting from separate genetic recombination events[J].Transfusion,2004,44:853-858.
[8] CHERIF-ZAHAR B,RAYNAL V,GANE P,et al.Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency[J].Nat Genet,1996,12:168-168.
[9] DANIELS G.The molecular genetics of blood group polymorphism[J].Transpl Immunol,2005,14:143-153.
[10] REID M E,LOMAS-FRANCIS C.The blood group antigen facts book[M].2nd New York:Elsevier Academic Press,2004.
[11] LUBENKO A,BURSLEM S,FAIRCLOUGH L M,et al.A New Qualitative Variant of the RhE Antigen Revealed by Heterogeneity among Anti-E Sera[J].Vox Sanguinis,60:235-240.
[12] SCOTT M L.Rh serology:co-ordinator`s report.4th Internatioal Workshop Monoclonal Antibodies against Human Red Cell Surface Antigens,Paris[J].Transfus Clin Biol,2002,9:23-29.
[13] PHAM B N,PEYRARD T,JUSZCZAK G,et al (2009).Heterogeneous molecular background of the weak C,VS+,hrB-,HrB-phenotype in black persons[J].Transfusion,49:495-504.
[14] BURTON N M,ANSTEE D J.Structure,function and signi?cance of Rh proteins in red cells[J].Curr pin Hematol,2008,15:625-630.
[15] NOIZAT-PIRENNE F,MOURO I,LE PENNEC P,et al.Molecular basis of category EIV variant phenotype[J].Transfusion,1999,39:103S-103S.
[16] DSCHER A,VOGT C,BITTNER R,et al.RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany[J].Transfusion,49:1803-1811.
[17] BUGERT P,SCHARBERG E A,GEISEN C,et al.RhCE protein variants in Southwestern Germany detected by serologic routine testing[J].Transfusion,2009,49:1793-1802.
[18] PHAM BN,PEYRARD T,JUSZCZAK G,et al.Analysis of RhCE variants among 806 individuals in France:considerations for transfusion safety,with emphasis on patients with sickle cell disease[J].Transfusion,2011,51:1537-2995.
[19] PEYRARD T,PHAM BN,POUPEL S,et al.Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE*ceAR allele (ceAR) encodes a partial c antigen[J].Transfusion,2009,49:2406-2411.
[20] HALTER H C,LOMAS-FRANCIS C,FUCHISAWA A,et al.RHCE*ceCF and RHCE*ceAR each encode a partial c (RH4) antigen[J].Transfusion,2009,49:138A-139A.
[21] PHAM BN,PEYRARD T,JUSZCZAK G,et al.Alloanti-c (RH4) revealing that the (C) ces haplotype encodes a partial c antigen[J].Transfusion,2009,49:1329-1334.
[22] HIPSKY C H,LOMAS-FRANCIS C,FUCHISAWA A,et al.RHCE*ceCF encodes partial c and partial e but not CELO,an antigen antithetical to Crawford[J].Transfusion,2011,51:25-31.
[23] JEREMIAH Z A,MORDI A,BUSERI F I,et al.Frequencies of maternal red blood cell alloantibodies in Port Harcourt,Nigeria[J].Asian J Transfus Sci,2011,5:39-41.
[24] DAVID J,ANSTEEL.The relationship between blood groups and disease[J].Blood,2010,115:4635-4643.
[25] KITAZAWA J,NOLLET K,MORIOKA H,et al.Non-D Rh antibodies appearing after apheresis platelet transfusion:stimulation by red cells or microparticles?[J].Vox Sanguinis,2011,100:395-400.
[26] CHATTERJI K B.Importance of phenotyping PH-kell testing in India done in en-technology at aims[J].Vox Sanguinis,2007:60-61.
[27] BUGERT P,SCHARBERG E A,GEISEN C,et al.RhCE protein variants in Southwestern Germany detected by serologic routine testing[J].Transfusion,2009,49:1793-1802.
[28] FRANCE NP,KETTY LEE PY,PENNEC R.RHCE phenotypes in black individuals of Afro-Caribbean origin:identi?cation and transfusion safety[J].Blood,2002,100:4223-4231.
[29] ILONA H,LENKA V,KLARA V.Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in RHD-negative pregnancies[J].J Hist Cyto,2005:53:301-305.
[30] ILONA H,KLARA V,JINDRICH D,et al.Non-invasive determination of fetal c and E allele of RHCE gene via real-time PCR testing of extracellular DNA extracted from maternal plasma samples using QIAamp DSP Virus kit[J].J Turkish German Gynecol Assoc,2007,8:140-147.
[31] GEIFMAN-HOLTZMAN O,GROTEGUT C,GAU-GHAN J,et al.Noninvasive fetal RhCE genotyping from maternal blood.BJOG:An international[J].J Obst Gyna,2009,116:144-151.
[32] NOIZAT-PIRENNE F,MOURO I,LE PENNEC P-Y,et al.Two new alleles of the RHCE gene in Black individuals:the RHce allele ceMO and the RHcE allele cEMI[J].Bri J Haematol,2001,113:672-679.
-
计量
- 文章访问数: 107
- PDF下载数: 119
- 施引文献: 0
下载: