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Volumn 25, Issue 12, 2005, Pages 1079-1083

Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies

Author keywords

Alloimmunization; Haemolytic disease of the newborn; Maternal plasma; RHCE gene; RHD Gene

Indexed keywords

ALLOANTIBODY; RHESUS C ANTIBODY; RHESUS D ANTIBODY; RHESUS E ANTIBODY;

EID: 29544445252     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1282     Document Type: Article
Times cited : (21)

References (13)
  • 1
    • 0031873052 scopus 로고    scopus 로고
    • Antenatal genotyping of the blood groups of the fetus
    • Avent ND. 1998. Antenatal genotyping of the blood groups of the fetus. Vox Sang 74: 365-374.
    • (1998) Vox Sang , vol.74 , pp. 365-374
    • Avent, N.D.1
  • 2
    • 0034651012 scopus 로고    scopus 로고
    • The Rh blood group system: A review
    • Avent ND, Reid ME. 2000. The Rh blood group system: a review. Blood 95: 375-387.
    • (2000) Blood , vol.95 , pp. 375-387
    • Avent, N.D.1    Reid, M.E.2
  • 3
    • 0025860203 scopus 로고
    • Epidemiology of Rh hemolytic disease of the newborn in the United States
    • Chavez GF, Mulinare J, Edmonds LD. 1991. Epidemiology of Rh hemolytic disease of the newborn in the United States. JAMA 2651: 3270-3274.
    • (1991) JAMA , vol.2651 , pp. 3270-3274
    • Chavez, G.F.1    Mulinare, J.2    Edmonds, L.D.3
  • 4
    • 0025723965 scopus 로고
    • Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis
    • Colin Y, Cherif-Zahar B, Le Van Kim C, Raynal V, Van Huffel V, Cartron JP. 1991. Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis. Blood 78: 2747-2752.
    • (1991) Blood , vol.78 , pp. 2747-2752
    • Colin, Y.1    Cherif-Zahar, B.2    Le Van Kim, C.3    Raynal, V.4    Van Huffel, V.5    Cartron, J.P.6
  • 5
    • 0034057403 scopus 로고    scopus 로고
    • Multiplex and real-time quantitative PCR on fetal DNA in maternal plasma: A comparison with fetal cells isolated from maternal blood: In circulating DNA in plasma
    • Hahn S, Zhong XY, Burk MR, Troeger C, Holzgreve W. 2000. Multiplex and real-time quantitative PCR on fetal DNA in maternal plasma: a comparison with fetal cells isolated from maternal blood: in Circulating DNA in Plasma. Ann N Y Acad Sci 906: 148-152.
    • (2000) Ann N Y Acad Sci , vol.906 , pp. 148-152
    • Hahn, S.1    Zhong, X.Y.2    Burk, M.R.3    Troeger, C.4    Holzgreve, W.5
  • 6
    • 14844304701 scopus 로고    scopus 로고
    • Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in Rh D negative pregnancies
    • Hromadnikova I, Vechetova L, Vesela K, Benesova B, Doucha J, Vlk R. 2005. Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in Rh D negative pregnancies. J Histochem Cytochem 53: 301-305.
    • (2005) J Histochem Cytochem , vol.53 , pp. 301-305
    • Hromadnikova, I.1    Vechetova, L.2    Vesela, K.3    Benesova, B.4    Doucha, J.5    Vlk, R.6
  • 7
    • 0037341393 scopus 로고    scopus 로고
    • Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination
    • Hromadnikova I, Houbova B, Hridelova D. et al. 2003. Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination. Prenat Diagn 23: 235-238.
    • (2003) Prenat Diagn , vol.23 , pp. 235-238
    • Hromadnikova, I.1    Houbova, B.2    Hridelova, D.3
  • 8
    • 0036889722 scopus 로고    scopus 로고
    • Prediction of fetal RhD and Rh CcEe phenotype from maternal plasma with real-time polymerase chain reaction
    • Legler TJ, Lynen R, Maas JH, Pindur G, Kulenkampff D, Suren A. 2002. Prediction of fetal RhD and Rh CcEe phenotype from maternal plasma with real-time polymerase chain reaction. Transfus Apheresis Sci 27: 217-223.
    • (2002) Transfus Apheresis Sci , vol.27 , pp. 217-223
    • Legler, T.J.1    Lynen, R.2    Maas, J.H.3    Pindur, G.4    Kulenkampff, D.5    Suren, A.6
  • 9
    • 0032506669 scopus 로고    scopus 로고
    • Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
    • Lo YMD, Hjelm NM, Fidler C. et al. 1998a. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 339: 1734-1738.
    • (1998) N Engl J Med , vol.339 , pp. 1734-1738
    • Lo, Y.M.D.1    Hjelm, N.M.2    Fidler, C.3
  • 10
    • 0347898005 scopus 로고    scopus 로고
    • Quantitative analysis of fetal DNA in maternal plasma and serum. Implications for noninvasive prenatal diagnosis
    • Lo YMD, Tein MSC, Lau TK. et al. 1998b. Quantitative analysis of fetal DNA in maternal plasma and serum. Implications for noninvasive prenatal diagnosis. Am J Hum Genet 62: 768-775.
    • (1998) Am J Hum Genet , vol.62 , pp. 768-775
    • Lo, Y.M.D.1    Tein, M.S.C.2    Lau, T.K.3
  • 11
    • 0030742588 scopus 로고    scopus 로고
    • The RHD gene is highly detectable in RhD-negative Japanese donors
    • Okuda H, Kawano M, Iwamoto S. et al. 1997. The RHD gene is highly detectable in RhD-negative Japanese donors. J Clin Invest 100: 373-379.
    • (1997) J Clin Invest , vol.100 , pp. 373-379
    • Okuda, H.1    Kawano, M.2    Iwamoto, S.3
  • 12
    • 0036628978 scopus 로고    scopus 로고
    • Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype
    • Rodrigues A, Rios M, Pellegrino J Jr, Costa FF, Castilho L. 2002. Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype. Braz J Med Biol Res 35: 767-773.
    • (2002) Braz J Med Biol Res , vol.35 , pp. 767-773
    • Rodrigues, A.1    Rios, M.2    Pellegrino Jr., J.3    Costa, F.F.4    Castilho, L.5
  • 13
    • 0033957696 scopus 로고    scopus 로고
    • The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype
    • Singleton BK, Green CA, Avent ND. et al. 2000. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype. Blood 95: 12-18.
    • (2000) Blood , vol.95 , pp. 12-18
    • Singleton, B.K.1    Green, C.A.2    Avent, N.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.