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Volumn 20, Issue 6, 2000, Pages 453-458

The applicability of different PCR-based methods for fetal RHD and K1 genotyping: A prospective study

Author keywords

Fetal blood group typing; K1; Multiplex PCR; RHD

Indexed keywords

RHESUS D ANTIGEN;

EID: 0034045921     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0223(200006)20:6<453::AID-PD858>3.0.CO;2-0     Document Type: Article
Times cited : (6)

References (40)
  • 1
    • 0033656961 scopus 로고    scopus 로고
    • Chorion villus sampling versus amniocentesis for prenatal diagnosis (Cochrane Review)
    • Update Software: Oxford
    • Alfirevic Z, Gosden C, Neilson JP. 1998. Chorion villus sampling versus amniocentesis for prenatal diagnosis (Cochrane Review). In The Cochrane Library, Issue 3. Update Software: Oxford.
    • (1998) The Cochrane Library , Issue.3
    • Alfirevic, Z.1    Gosden, C.2    Neilson, J.P.3
  • 2
    • 0027293541 scopus 로고
    • Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals
    • Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA, Lublin DM. 1993. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. Blood 82: 651-655.
    • (1993) Blood , vol.82 , pp. 651-655
    • Arce, M.A.1    Thompson, E.S.2    Wagner, S.3    Coyne, K.E.4    Ferdman, B.A.5    Lublin, D.M.6
  • 3
    • 0029949995 scopus 로고    scopus 로고
    • Kell typing by allele-specific PCR (ASP)
    • Avent ND, Martin PG. 1996. Kell typing by allele-specific PCR (ASP). Br J Haemat 93: 728-730.
    • (1996) Br J Haemat , vol.93 , pp. 728-730
    • Avent, N.D.1    Martin, P.G.2
  • 4
    • 0342531273 scopus 로고    scopus 로고
    • Molecular basis of the DVI variant phenotype: Evidence that a RHD deletion event does not generate all cDVIE haplotypes
    • 3us P1C7, 1996 (abstract)
    • Avent ND, Jones JW, Liu W, Scott ML, Voak D, Pisacka M, Watt J, Fletcher A. 1996. Molecular basis of the DVI variant phenotype: evidence that a RHD deletion event does not generate all cDVIE haplotypes. Tranf Clin et Biol 3: 3us P1C7, 1996 (abstract).
    • (1996) Tranf Clin et Biol , vol.3
    • Avent, N.D.1    Jones, J.W.2    Liu, W.3    Scott, M.L.4    Voak, D.5    Pisacka, M.6    Watt, J.7    Fletcher, A.8
  • 9
    • 0027993037 scopus 로고
    • Serotype switching in a partially deleted RhD gene
    • Blunt T, Daniels G, Carritt B. 1994. Serotype switching in a partially deleted RhD gene. Vox Sang 67: 397-401.
    • (1994) Vox Sang , vol.67 , pp. 397-401
    • Blunt, T.1    Daniels, G.2    Carritt, B.3
  • 10
    • 0030853605 scopus 로고    scopus 로고
    • Differences between RhD-negative Africans and RhD-negative Europeans
    • Daniels G, Green C, Smart E. 1997. Differences between RhD-negative Africans and RhD-negative Europeans. Lancet 350: 862.
    • (1997) Lancet , vol.350 , pp. 862
    • Daniels, G.1    Green, C.2    Smart, E.3
  • 11
    • 0030222022 scopus 로고    scopus 로고
    • Determination of fetal RhD status from uncultured amniocytes
    • Dildy GA, Jackson GM, Ward K. 1996. Determination of fetal RhD status from uncultured amniocytes. Obstet Gynecol 88: 207-210.
    • (1996) Obstet Gynecol , vol.88 , pp. 207-210
    • Dildy, G.A.1    Jackson, G.M.2    Ward, K.3
  • 12
    • 0027787872 scopus 로고
    • Complications of ultrasound-guided percutaneous umbilical blood sampling: Analysis of a series of 341 cases and review of the literature
    • Duchatel F, Aury JF, Mennesson B. 1993. Complications of ultrasound-guided percutaneous umbilical blood sampling: analysis of a series of 341 cases and review of the literature. Eur J Obstet Gynecol Reprod Biol 52: 95-104.
    • (1993) Eur J Obstet Gynecol Reprod Biol , vol.52 , pp. 95-104
    • Duchatel, F.1    Aury, J.F.2    Mennesson, B.3
  • 15
    • 0028070609 scopus 로고
    • Clinical utility of fetal RhD typing in alloimmunized pregnancies by means of polymerase chain reaction on amniocytes or chorionic villi
    • Fisk NM, Bennett P, Warwick RM, Letsky EA, Welch R. 1994. Clinical utility of fetal RhD typing in alloimmunized pregnancies by means of polymerase chain reaction on amniocytes or chorionic villi. Am J Obstet Gynecol 171: 50-54.
    • (1994) Am J Obstet Gynecol , vol.171 , pp. 50-54
    • Fisk, N.M.1    Bennett, P.2    Warwick, R.M.3    Letsky, E.A.4    Welch, R.5
  • 17
    • 0025899530 scopus 로고
    • Amniocentesis or chorionic villus sampling for prenatal genetic testing: A decision analysis
    • Heckerling PS, Verp MS. 1991. Amniocentesis or chorionic villus sampling for prenatal genetic testing: a decision analysis. J Clin Epidemiol 44: 657-670.
    • (1991) J Clin Epidemiol , vol.44 , pp. 657-670
    • Heckerling, P.S.1    Verp, M.S.2
  • 18
    • 0030017853 scopus 로고    scopus 로고
    • Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers
    • Hessner MJ, McFarland JG, Endean DJ. 1996. Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers. Transfusion 36: 495-499.
    • (1996) Transfusion , vol.36 , pp. 495-499
    • Hessner, M.J.1    McFarland, J.G.2    Endean, D.J.3
  • 19
    • 0028241841 scopus 로고
    • Three unrelated RhD gene polymorphisms identified among blood donors with Rhesus CCee (r′r′) phenotypes
    • Hyland CA, Wolter LC, Saul A. 1994. Three unrelated RhD gene polymorphisms identified among blood donors with Rhesus CCee (r′r′) phenotypes. Blood 84: 321-324.
    • (1994) Blood , vol.84 , pp. 321-324
    • Hyland, C.A.1    Wolter, L.C.2    Saul, A.3
  • 20
    • 0028936247 scopus 로고
    • Molecular basis of the Kell (K1) phenotype
    • Lee S, Wu X, Reid M, Zelinski T, Redman C. 1995. Molecular basis of the Kell (K1) phenotype. Blood 85: 912-916.
    • (1995) Blood , vol.85 , pp. 912-916
    • Lee, S.1    Wu, X.2    Reid, M.3    Zelinski, T.4    Redman, C.5
  • 21
    • 0028070411 scopus 로고
    • PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease
    • Le Van Kim C, Mouro I, Brossard Y, Chavinie J, Cartron JP, Colin Y. 1994. PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease. Br J Haemat 8864: 193-195.
    • (1994) Br J Haemat , vol.8864 , pp. 193-195
    • Le Van Kim, C.1    Mouro, I.2    Brossard, Y.3    Chavinie, J.4    Cartron, J.P.5    Colin, Y.6
  • 26
    • 0030158309 scopus 로고    scopus 로고
    • Development of a PCR-based diagnostic assay for the determination of the KEL genotype in donor blood samples
    • Murphy MT, Fraser RH, Goddard JP. 1996. Development of a PCR-based diagnostic assay for the determination of the KEL genotype in donor blood samples. Transfus Med 6: 133-137.
    • (1996) Transfus Med , vol.6 , pp. 133-137
    • Murphy, M.T.1    Fraser, R.H.2    Goddard, J.P.3
  • 29
    • 0029967852 scopus 로고    scopus 로고
    • DNA-based Rhesus typing: Simultaneously determination of RHC and RHD status using the polymerase chain reaction
    • Poulter M, Kemp TJ, Carritt B. 1996. DNA-based Rhesus typing: simultaneously determination of RHC and RHD status using the polymerase chain reaction. Vox Sang 70: 164-168.
    • (1996) Vox Sang , vol.70 , pp. 164-168
    • Poulter, M.1    Kemp, T.J.2    Carritt, B.3
  • 32
    • 0343836467 scopus 로고
    • Molecular basis of the lack of expression of some Rh epitopes in D category phenotypes
    • Rouillac C, Mouro I, Beolet M, Cartron JP, Le Van Kim C. Colin Y. 1994, Molecular basis of the lack of expression of some Rh epitopes in D category phenotypes. Br J Haemat 87 (Suppl 1): 150.
    • (1994) Br J Haemat , vol.87 , Issue.SUPPL. 1 , pp. 150
    • Rouillac, C.1    Mouro, I.2    Beolet, M.3    Cartron, J.P.4    Le Van Kim, C.5    Colin, Y.6
  • 33
    • 0029059940 scopus 로고
    • Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alterations of D epitopes
    • Rouillac C, Colin Y, Hughes-Jones NC, Beolet M, d'Ambrioso AM, Cartron J-P, Le van Kim C. 1995a. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alterations of D epitopes. Blood 85: 2937-2944.
    • (1995) Blood , vol.85 , pp. 2937-2944
    • Rouillac, C.1    Colin, Y.2    Hughes-Jones, N.C.3    Beolet, M.4    D'Ambrioso, A.M.5    Cartron, J.-P.6    Le Van Kim, C.7
  • 34
    • 0028963904 scopus 로고
    • Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes
    • Rouillac C, Le Van Kim C, Blancher A, Roubinet F, Cartron JP, Colin Y. 1995b. Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes. Br J Haemat 89: 424-426.
    • (1995) Br J Haemat , vol.89 , pp. 424-426
    • Rouillac, C.1    Le Van Kim, C.2    Blancher, A.3    Roubinet, F.4    Cartron, J.P.5    Colin, Y.6
  • 38
    • 0028804663 scopus 로고
    • Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic disease
    • Spence WC, Maddalena A, Demers DB, Bick DP. 1995. Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic disease. Obstet Gynecol 85: 296-298.
    • (1995) Obstet Gynecol , vol.85 , pp. 296-298
    • Spence, W.C.1    Maddalena, A.2    Demers, D.B.3    Bick, D.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.