Large-Scale Pre-Diagnosis Study of Fetal RHD Genotyping by PCR on Plasma DNA from RhD-Negative Pregnant Women
Tóm tắt
Từ khóa
Tài liệu tham khảo
Brossard Y, Parnet-Mathieu F, Larsen M. Incompatibilités foeto-niaternelles érythrocytaires. In: Transfusion sanguine: une approche sécuritaire. Montrouge: John Libbey, 2000: 290–318
Colin Y, Chérif-Zahar B, Le Van Kim C, et al. Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis. Blood 1991; 78: 2747–52
Bennett PR, Le Van Kim C, Colin Y, et al. Prenatal determination of fetal RhD type by DNA amplification. N Engl J Med 1993; 329: 607–10
Lo YM, Bowell PJ, Selinger M, et al. Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers. Lancet 1993; 341: 1147–8
Rouillac C, Colin Y, Hughes-Jones NC, et al. Transcript analysis of D category phenotypes predicts hybrid RhD-CE-D proteins associated with alteration of D epitopes. Blood 1995; 85: 2937–44
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 RhD-negative blood group phenotype. Blood 2000; 95: 12–8
Simsek S, Faas BHW, Bleeker PMM, et al. Rapid RhD genotyping by polymerase chain reaction-based amplification of DNA. Blood 1995; 85: 2975–80
Aubin JT, Le Van Kim C, Mouro I, et al. Specificity and sensitivity of RHD genotyping methods by PCR-based DNA amplification. Br J Haematol 1997; 98: 356–64
Maaskant-van Wijk PA, Faas BH, de Ruitjer JA, et al. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons [published erratum appears in Transfusion 1999 May, 39 (5): 546]. Transfusion 1998; 38: 1015–21
Murray JC, Karp LE, Williamson LA, et al. Rh isoimmunisation related to amniocentesis. Am J Med Genet 1983; 16: 527–34
Pratt GA, Bowell PJ, Mackenzie IZ, et al. Production of additional atypical alloantibodies in Rh(D)-sensitized pregnancies managed by intrauterine investigation methods. Clin Lab Haematol 1989; 11: 241–8
Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997; 350: 485–7
Lo YM, Hjelm NM, Fidler C, et al. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 1998; 339: 1734–8
Zhang J, Filder C, Murphy MF, et al. Determination of fetal RHD status by maternal plasma DNA analysis. Ann N Y Acad Sci 2000; 906: 153–5
Avent ND, Finning KM, Martin PG, et al. Prenatal determination of fetal blood group status. Vox Sang 2000; 78 Suppl. 2: 155–62
Zhong XY, Holzgreve W, Hahn S. Risk free simultaneous prenatal identification of fetal Rhesus D status and sex by multiplex real-time PCR using cell free DNA in maternal plasma. Swiss Med Wkly 2001; 131: 70–4
Costa JM, Giovangrandi Y, Ernault P, et al. Fetal RHD genotyping in maternal serum during the first trimester of pregnancy. Br J Haematol 2002; 119: 255–60
van der Schoot CE, Tax GHM, Rijnders RJP, et al. Prenatal typing of Rh and Kell blood group system antigens: the edge of a watershed. Transfus Med Rev 2003; 17: 31–44
Faas BH, Beuling EA, Christiaens GC, et al. Detection of fetal RHD-specific sequences in maternal plasma [letter]. Lancet 1998; 352: 1196
Zhong XY, Holzgreve W, Hahn S. Detection of fetal Rhesus D and sex using fetal DNA from maternal plasma by multiplex polymerase chain reaction. Br J Obstret Gynaecol 2000; 107: 766–9
Finning KM, Martin PG, Soothill PW, et al. Prediction of fetal D status from maternal plasma: introduction of a new invasive fetal RHD genotyping service. Transfusion 2002; 42: 1079–85
Legler TJ, Lynen R, Maas JH, et al. Prediction of fetal RhD and RhCcEe phenotype from maternal plasma with real-time polymerase chain reaction. Transfus Apheresis Sci 2002; 27: 217–23
Huang CH, Liu PZ, Cheng JG. Molecular biology and genetics of the Rh blood group system. Semin Hematol 2000; 37: 150–65
Honda H, Miharu N, Ohashi Y, et al. Successful diagnosis of fetal gender using conventional PCR analysis of maternal serum. Clin Chem 2001; 47: 41–6
Lo YM, Tein MS, Lau TK, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet 1998; 62: 768–75
Wei C, Sailer DN, Sutherland JW. Detection and quantification by homogeneous PCR of cell-free fetal DNA in maternal plasma. Clin Chem 2001; 47: 336–8
Randen I, Hauge R, Kjeldsen-Kragh J, et al. Prenatal genotyping of RHD and SRY using maternal blood. Vox Sang 2003; 85: 300–6
Tang NL, Leung TN, Zhang J, et al. Detection of fetal-derived paternally inherited X-chromosome polymorphisms in maternal plasma. Clin Chem 1999; 45: 2033–5
Finning K, Martin P, Avent ND. Noninvasive prenatal diagnosis of fetal blood group status. Transfus Med 1999; 9 Suppl. 1: 32
Pertl B, Sekizawa A, Samura O, et al. Detection of male and female fetal DNA in maternal plasma by multiplex fluorescent polymerase chain reaction amplification of short tandem repeats. Hum Genet 2000; 95: 45–9
Lo YM, Lau TK, Zhang J, et al. Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy 21. Clin Chem 1999; 45: 1747–51
Blunt T, Daniels G, Carritt B. Serotype switching in a partially deleted RHD gene. Vox Sang 1994; 67: 397–401
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