메뉴 건너뛰기




Volumn 51, Issue 3, 2011, Pages 570-573

RhD variant caused by an in-frame triplet duplication in the RHD gene

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; REAGENT; RHESUS D ANTIBODY;

EID: 79952457222     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/j.1537-2995.2010.02856.x     Document Type: Article
Times cited : (10)

References (12)
  • 1
    • 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. Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by southern analysis. Blood 1991;78:2747-52.
    • (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
  • 3
    • 1442275829 scopus 로고    scopus 로고
    • Review: The molecular basis of the Rh blood group phenotypes
    • Wagner FF, Flegel WA. Review: the molecular basis of the Rh blood group phenotypes. Immunohematology 2004;20:23-36. (Pubitemid 38292745)
    • (2004) Immunohematology , vol.20 , Issue.1 , pp. 23-36
    • Wagner, F.F.1    Flegel, W.A.2
  • 5
    • 0036150975 scopus 로고    scopus 로고
    • Molecular biology of partial D and weak D: Implications for blood bank practice
    • Flegel WA, Wagner FF. Molecular biology of partial D and weak D: implications for blood bank practice. Clin Lab 2002;48:53-9. (Pubitemid 34110584)
    • (2002) Clinical Laboratory , vol.48 , Issue.1-2 , pp. 53-59
    • Flegel, W.A.1    Wagner, F.F.2
  • 6
    • 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, Martin PG, Smart E, Daka A, Narter-Olaga EG, Hawthorne LM, Daniels G. 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 2000;95:12-18. (Pubitemid 30017219)
    • (2000) Blood , vol.95 , Issue.1 , pp. 12-18
    • Singleton, B.K.1    Green, C.A.2    Avent, N.D.3    Martin, P.G.4    Smart, E.5    Daka, A.6    Narter-Olaga, E.G.7    Hawthorne, L.M.8    Daniels, G.9
  • 7
    • 54349129765 scopus 로고    scopus 로고
    • Gene symbol: RHD. Disease: rhesus blood group variation. Human genetics
    • Pereira JC, Rodrigues MJ, Chabert T. Gene symbol: RHD. Disease: rhesus blood group variation. Human genetics. Hum Genet 2008;124:306.
    • (2008) Hum Genet , vol.124 , pp. 306
    • Pereira, J.C.1    Rodrigues, M.J.2    Chabert, T.3
  • 8
    • 0033987736 scopus 로고    scopus 로고
    • Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
    • DOI 10.1002/(SICI)1098-1004(200001)15:1<7::AID-HUMU4>3.0.CO;2-N
    • den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat 2000;15:7-12. (Pubitemid 30036162)
    • (2000) Human Mutation , vol.15 , Issue.1 , pp. 7-12
    • Den, D.J.T.1    Antonarakis, S.E.2
  • 12
    • 69249174057 scopus 로고    scopus 로고
    • RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany
    • Döscher A, Vogt C, Bittner R, Gerdes I, Petershofen EK, Wagner FF. RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany. Transfusion 2009;49:1803-11.
    • (2009) Transfusion , vol.49 , pp. 1803-1811
    • Döscher, A.1    Vogt, C.2    Bittner, R.3    Gerdes, I.4    Petershofen, E.K.5    Wagner, F.F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.