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Volumn 368, Issue 1-2, 2006, Pages 195-198

Molecular detection of Spanish δβ-thalassemia associated with β-thalassemia identified during prenatal diagnosis

Author keywords

Thalassemia; Prenatal diagnosis; Spanish thalassemia

Indexed keywords

BETA GLOBIN; CD37 ANTIGEN; CD39 ANTIGEN; CD6 ANTIGEN; DNA;

EID: 33646834790     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2005.12.041     Document Type: Article
Times cited : (4)

References (16)
  • 2
    • 0037057597 scopus 로고    scopus 로고
    • Effect of consanguinity on screening for talasemia
    • Cao A., and Galanello R. Effect of consanguinity on screening for talasemia. N Engl J Med 347 (2002) 1200-1202
    • (2002) N Engl J Med , vol.347 , pp. 1200-1202
    • Cao, A.1    Galanello, R.2
  • 3
    • 0033547527 scopus 로고    scopus 로고
    • Alteraciones moleculares de las talasemias en España. Revisión de los estudios existentes
    • Moreno I., Bolufer P., and Pérez M. Alteraciones moleculares de las talasemias en España. Revisión de los estudios existentes. Med Clín (Barc) 113 (1999) 789-794
    • (1999) Med Clín (Barc) , vol.113 , pp. 789-794
    • Moreno, I.1    Bolufer, P.2    Pérez, M.3
  • 4
    • 33646839992 scopus 로고
    • Heterogeneity of thalassemia major
    • Wolff J.A., and Ignatov V.G. Heterogeneity of thalassemia major. Am J Dis Child 105 (1963) 224-235
    • (1963) Am J Dis Child , vol.105 , pp. 224-235
    • Wolff, J.A.1    Ignatov, V.G.2
  • 6
    • 0014559289 scopus 로고
    • F-Thalassemia: a study of thirty-one families with simple heterozygotes and combinations of F-thalassemia with A2-thalassemia
    • Stamatoyannopoulos G., Fessas P., and Papayannopoulou T. F-Thalassemia: a study of thirty-one families with simple heterozygotes and combinations of F-thalassemia with A2-thalassemia. Am J Med 47 (1969) 194-208
    • (1969) Am J Med , vol.47 , pp. 194-208
    • Stamatoyannopoulos, G.1    Fessas, P.2    Papayannopoulou, T.3
  • 7
    • 0015842549 scopus 로고
    • The clinical and haematological findings in children inheriting two types of thalassaemia: high-A2, type beta-thalassaemia, and high F-type or delta-beta-thalassaemia
    • Kattamis C., Metaxotou-Mavromati A., Karamboula K., Nasika E., and Lehmann H. The clinical and haematological findings in children inheriting two types of thalassaemia: high-A2, type beta-thalassaemia, and high F-type or delta-beta-thalassaemia. Br J Haematol 25 (1973) 375-384
    • (1973) Br J Haematol , vol.25 , pp. 375-384
    • Kattamis, C.1    Metaxotou-Mavromati, A.2    Karamboula, K.3    Nasika, E.4    Lehmann, H.5
  • 9
    • 0035136908 scopus 로고    scopus 로고
    • Two thalassemia intermedia patients with δβ/β-thalassemia and a deletional type α-thalassemia
    • Li Z., Liu L., Zhao Y., Zhong X., and Xu X. Two thalassemia intermedia patients with δβ/β-thalassemia and a deletional type α-thalassemia. Haematologica 86 (2001) 108
    • (2001) Haematologica , vol.86 , pp. 108
    • Li, Z.1    Liu, L.2    Zhao, Y.3    Zhong, X.4    Xu, X.5
  • 11
    • 0036436890 scopus 로고    scopus 로고
    • Rapid detection of the major Mediterranean β-thalassaemia mutations by real-time PCR using fluorophore-labelled hybridization probes
    • Moreno I., Bolufer P., Pérez M.L., Barragán E., and Sanz M.A. Rapid detection of the major Mediterranean β-thalassaemia mutations by real-time PCR using fluorophore-labelled hybridization probes. Br J Haematol 119 (2002) 554-557
    • (2002) Br J Haematol , vol.119 , pp. 554-557
    • Moreno, I.1    Bolufer, P.2    Pérez, M.L.3    Barragán, E.4    Sanz, M.A.5
  • 15
    • 0025905754 scopus 로고
    • δβ Thalassemia and hereditary persistence of fetal hemoglobin
    • Bollekens J.A., and Forget B.G. δβ Thalassemia and hereditary persistence of fetal hemoglobin. Hematol Oncol Clin North Am 5 (1991) 399-422
    • (1991) Hematol Oncol Clin North Am , vol.5 , pp. 399-422
    • Bollekens, J.A.1    Forget, B.G.2
  • 16
    • 0028214609 scopus 로고
    • Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification
    • Craig J.E., Barnetson R.A., Prior J., Raven J.L., and Thein S.L. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood 15 83 (1994) 1673-1682
    • (1994) Blood , vol.15 , Issue.83 , pp. 1673-1682
    • Craig, J.E.1    Barnetson, R.A.2    Prior, J.3    Raven, J.L.4    Thein, S.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.