[1] LE VAN KIM C,COLIN Y,CARTRON J P.Rh proteins:key structural and functional components of the red cell membrane[J].Blood Rev,2006,20(2):93-110.
[2] PHAM B N,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(6):1249-1260.
[3] ANDERSON R,VEGE S,AESCHLIMANN J,et al.RHCE*02 (c.148G>A,p.Val50Ile) allele with silenced RHCE*Ce expression[J].Transfusion,2020,60(8):E23-E24.
[4] DEZAN M R,OLIVEIRA V B,GOMES Ç N,et al.High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype[J].J Clin Lab Anal,2018,32(9):e22596.
[5] EL HOUSSE H,EL WAFI M,OUABDELMOUMENE Z,et al.Comprehensive phenotypic and molecular investigation of RHD and RHCE variants in Moroccan blood donors[J].Blood Transfus,2019,17(2):151-156.
[6] SHI J,LUO Y.Effects of RHD gene polymorphisms on distinguishing weak D or DEL from RHD- in blood donation in a Chinese population[J].Mol Genet Genom Med,2019,7(6):e00681.
[7] MÖLLER M,JÖUD M,STORRY J R,et al.Erythrogene:a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project[J].Blood Adv,2016,1(3):240-249.
[8] POULTER M,KEMP T J,CARRITT B.DNA-based Rhesus typing:simultaneous determination of RHC and RHD status using the polymerase chain reaction[J].Vox Sang,1996,70(3):164-168.
[9] DANIELS G.Human blood groups[M].3rd ed.Chichester:Wiley-Blackwell,2013.
[10] PHAM B N,RAMELET S,WIBAUT B,et al.Molecular background of novel silent RHCE alleles[J].Transfusion,2013,53(11pt2):2990-2999.
[11] SILVY M,BARRAULT A,VELLIQUETTE R W,et al.RHCE*Ce734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents[J].Transfusion,2013,53(5):955-961.
[12] PHAM B N,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(6):1249-1260.
[13] 张秀铮,张韦,王守燕,等.Rh缺失型D-基因检测及家系成员D抗原、Rh17抗原定量分析[J].中国输血杂志,2014,27(3):263-265.
[14] 伍伟健,郭如华,余晋林.Rh缺失型D——个体及其家系成员基因分型及遗传背景分析[J].中国生物制品学杂志,2010,23(8):881-884.
[15] 左琴琴,张薇薇,褚晓月,等.两例D——个体的血清学鉴定和基因分析[J].中国输血杂志,2020,33(6):558-561.
[16] FLATT J F,MUSA R H,AYOB Y,et al.Study of the D—phenotype reveals erythrocyte membrane alterations in the absence of RHCE[J].Br J Haematol,2012,158(2):262-273.
[17] 李明浩,杨佳璇,李艾静,等.1例部分D表型献血者RhD抗原表位及分子机制研究[J].临床输血与检验,2022,24(1):16-21.
[18] 赵瑛,李双玉,黄娴,等.Rh缺失型D(D——)血型的免疫学检测及稀有血型库分析[J].细胞与分子免疫学杂志,2021,37(2):164-167.
[19] 李楚,张勇萍,张从利,等.Rh缺失型-D-表型的血型血清学检测及其临床意义分析[J].细胞与分子免疫学杂志,2018,34(5):448-451.
[20] 李翠莹,李小薇.胎儿新生儿溶血病实验室检测专家共识[J].临床输血与检验,2021,23(1):20-23,28.
[21] 彭沫溱,姚富柱,罗臻,等.Rh缺失型D——导致新生儿溶血病的血液免疫学分析及家系调查[J].临床血液学杂志,2019,32(6):436-439. |
