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Volumn 94, Issue 8, 2009, Pages 1157-1159

Severe intrauterine anemia: A new form of εγγδβ thalassemia presenting in utero in a Norwegian family

Author keywords

Intrauterine anemia; Norwegian family; Thalassemia

Indexed keywords

BETA GLOBIN; HEMOGLOBIN;

EID: 68049142287     PISSN: 03906078     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.2009.007534     Document Type: Article
Times cited : (13)

References (8)
  • 1
    • 29144480573 scopus 로고    scopus 로고
    • Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification
    • Harteveld CL, Voskamp A, Phylipsen M, Akkermans N, den Dunnen JT, White SJ, et al. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification. J Med Genet 2005;42:922-31.
    • (2005) J Med Genet , vol.42 , pp. 922-931
    • Harteveld, C.L.1    Voskamp, A.2    Phylipsen, M.3    Akkermans, N.4    den Dunnen, J.T.5    White, S.J.6
  • 3
    • 20044391420 scopus 로고    scopus 로고
    • Heterogeneity of the εγδβ-thalassaemias: Characterization of three novel English deletions
    • Rooks H, Bergounioux J, Game L, Close JP, Osborne C, Best S, et al. Heterogeneity of the εγδβ-thalassaemias: characterization of three novel English deletions. Br J Haematol 2005;128:722-9.
    • (2005) Br J Haematol , vol.128 , pp. 722-729
    • Rooks, H.1    Bergounioux, J.2    Game, L.3    Close, J.P.4    Osborne, C.5    Best, S.6
  • 4
    • 0015516517 scopus 로고
    • γ-β thalassemia: A cause of hemolytic disease of the newborn
    • Kan YW, Forget BG, Nathan DG. γ-β thalassemia: a cause of hemolytic disease of the newborn. N Engl J Med 1972;286:129-34.
    • (1972) N Engl J Med , vol.286 , pp. 129-134
    • Kan, Y.W.1    Forget, B.G.2    Nathan, D.G.3
  • 5
    • 0025223668 scopus 로고
    • Molecular and hematologic characterization of Scottish-Irish type (εγδβ) ° thalassemia
    • Trent RJ, Williams BG, Kearney A, Wilkinson T, Harris PC. Molecular and hematologic characterization of Scottish-Irish type (εγδβ) ° thalassemia. Blood 1990;76:2132-8.
    • (1990) Blood , vol.76 , pp. 2132-2138
    • Trent, R.J.1    Williams, B.G.2    Kearney, A.3    Wilkinson, T.4    Harris, P.C.5
  • 6
  • 8
    • 50849115178 scopus 로고    scopus 로고
    • Genotype/phenotype correlation in hereditary spherocytosis
    • Iolascon A, Avvisati RA. Genotype/phenotype correlation in hereditary spherocytosis. Haematologica 2008;93:1283-8.
    • (2008) Haematologica , vol.93 , pp. 1283-1288
    • Iolascon, A.1    Avvisati, R.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.