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[1] FLEGEL W A,WAGNER F F.Molecular biology of partial D and weak D:implications for blood bank practice[J].Clin Lab,2002,48:53-59.
[2] WAGNER F F,GASSNER C,MVLLER T H,et al.Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features[J].Blood,1998,91:2157-2168.
[3] WESTHOFF C M,VEGE S,HALTER-HIPSKY C,et al.DⅢa and DⅢ type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles:clinical implications[J].Transfusion,2010,50:1303-1311.
[4] WAGNER F F,GASSNER C,MVLLER T H,et al.Molecular basis of weak D phenotypes[J].Blood,1999,93:385-393.
[5] CHOU S T,WESTHOFF C M,MVLLER T H,et al.Molecular biology of the Rh system:clinical considerations for transfusion in sickle cell disease[J].Hematology,2009:178-184.
[6] 赵桐茂.人类血型遗传学[M].北京;科学出版社,1987:105-106.
[7] SHAO C P,MAAS J H,SU Y Q,et al.Molecular background of Rh D-positive,D-negative,Del and weak D phenotypes in chinese[J].Vox Sanguinis,2002,83:156-161.
[8] MAKROO R N,RAINA V,CHOWDHRY M,et al.Weak D prevalence among Indina blood donors[J].Asian J Transf Sci,2010,4:137-139.
[9] FLEGEL W A,WAGNER F F.Molecular Genetics of RH[J].Vox Sang,2000,78:109-115.
[10] WAGNER F F,FLEGEL W A.RHD gene deletion occurred in the Rhesus box[J].Blood,2000,95:3662-3668.
[11] SCOTT M L,VOAK D,JONE J W,et al.A structural model for 30 Rh D epitopes based on serological and DNA sequence data from partial D phenotypes[J].TCB,1996,3:391-396.
[12] YAN L X,WU J J,ZHU F M,et al.Molecular basis of D variants in Chinese persons[J].Transfusion,2007,47:471-477.
[13] 吴俊杰,洪小珍,许先国,等.中国人Rh部分D表型的分子机理[J].中国实验血液学杂志,2006,14(3):587-591.
[14] 孙国栋,段现民,尹志柱,等.华北地区汉族人群Rh (D)抗原弱表现型个体的分子机制遗传研究[J].中国输血杂志,2007,20(2):108-112.
[15] WAGNER F F,KASSULKE D,KEROWGAN M,et al.Frequencies of the blood groups ABO,Rhesus,D category VI,Kell,and of clinnically relevant high-frequency antigens in South-West Germany[J].Infusionsther Transfusionsmed,1995,22:285-290.
[16] HELENE ANSART-PIRENNE H,ASSO-BONNET M,Le Pennec PY Roussel M,et al.RhD variants in Caucasians:conseqences for checking clinically relevant alleles[J].Transfusion,2004,44:1282-1286.
[17] DANIELS G.Rh blood group syetem[M].Human Blood Groups 2nd ed,Oxford:Blackwell,2002:195-274.
[18] Rhesus base.[2011-08-10] http://www.uni-ulm.de/~fwagner/RH/RB/.
[19] WAGNER F F,FROHMAJER A,LADEWIG B,et al.Weak D alleles express distinct phenotypes[J].Blood,2000,95:2699-2708.
[20] 孙国栋,段现民,张彦平,等.中国人群中发现的主要弱D型-弱D15个体的分子背景研究[J].中国实验血液学杂志,2006,15(5):1024-1028.
[21] LEGLER T J,WIEMANN V,OHTO H,et al.Dva category phenotype and genotype in janpanese families[J].Vox Sanguinis,2000,78:194-197.
[22] WAGNER F F,EICHER N I,JO[KG-*7/8] /RGENSEN J R,et al.DNB:a partial D with anti-D frequent in Central Europe[J].Blood,2002,100:2253-2256.
[23] WAGNER F F,FROHMAJER A,FLEGEL W A.RHD positive haplotypes in D negative Europeans[J].BMC Genetics,2001,2:10-18.
[24] 熊文,邵超鹏,周一炎.中国人特异性RHD基因定型方法的建立[J].中国输血杂志,2005,18(1):4-7.
[25] 李宏,宋宁,邓永福,等.四川地区汉族人群Rh (D)变异体分子机制研究[J].中国输血杂志,2010,23(5):365-372.
[26] STABENTHEINER S,DANZE M,NIKLAS N,et al,Overcoming methodical limits of standard RHD genotyping by next-generation sequencing[J].VoxSanguinis,2011,100:381-388.
[27] RODRIGUES A,RIOS M,PELLEGRINO J Jr,et al.Presence of the RHD pseudogene and the hybrid RHD-CE-DS gene in Brazilians with the D-negative phenotype[J].Braz Med BIOL Res,2002,35:767-773.
[28] 邵超鹏,熊文.一种新的RHD合子型直接测定方法[J].中华医学杂志,2000,84(9):736-739.
[29] 兰炯采,周华友,夏荣,等.Rhesus盒检测技术[J].中国实验血液学杂志,2005,13(6):1103-1105.
[30] NOIZAT-PIRENNE F,VERDINER M,LEJEALLE A,et al.Weak D phenotypes and transfusion safety:where do we stand in daily practice[J]?Transfusion,2007,47:1616-1620.
[31] DENOMME G A,WAGNER F F,FERNANDES B J,et al.Patial D,weak D types,and novel RHD alleles among 33,864 multiethnic patient:implication for anti-D alloimmunization and prevention[J].Transfusion,2005,45:1554-1560.
[32] PIERCE R,SCHUCKER J.Fatal Hydrops Fetalis Caused by Anti-D in a mother with partial D[J].Obstetrics Gynecol,2004,104:193-194.
[33] 邵智利,王更银,赵继芬,等.弱D型妊娠致抗-D引起的新生儿溶血病救治成功1例[J],中国输血杂志,2003,16(2):121-122.
[34] BACH-NGA,ROUSSEL M,PEYRARD T,et al.Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2:allo-or autoantibodies[J]?Transfusion,[2011-8-20] http://onlinelibrary.wiley.com/doi/10.1111/j.1537-2995.2011.03207.x/full.
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