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Volumn 144, Issue 3, 2004, Pages 391-393

Unusual phenotype of hemoglobin EE with hemoglobin H disease: A pitfall in clinical diagnosis and genetic counseling

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN;

EID: 1542406543     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2003.12.021     Document Type: Article
Times cited : (6)

References (12)
  • 1
    • 0007752751 scopus 로고    scopus 로고
    • Hemoglobinopathies in Southeast Asia: Molecular biology and clinical medicine
    • Fucharoen S, Winichagoon P. Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine. Hemoglobin 1997;21:299-319.
    • (1997) Hemoglobin , vol.21 , pp. 299-319
    • Fucharoen, S.1    Winichagoon, P.2
  • 3
    • 0023904470 scopus 로고
    • EF Bart's disease: Interaction of the abnormal alpha- and beta-globin genes
    • Fucharoen S, Winichagoon P, Thonglairuam V, Wasi P. EF Bart's disease: interaction of the abnormal alpha- and beta-globin genes. Eur J Haematol 1988;40:75-8.
    • (1988) Eur J Haematol , vol.40 , pp. 75-78
    • Fucharoen, S.1    Winichagoon, P.2    Thonglairuam, V.3    Wasi, P.4
  • 4
    • 0009066381 scopus 로고    scopus 로고
    • Hemoglobin E disorders
    • Nagel RL, editor. Cambridge, United Kingdom: Cambridge University Press
    • Fucharoen S. Hemoglobin E disorders. In: Nagel RL, editor. Disorders of Hemoglobin. Cambridge, United Kingdom: Cambridge University Press; 2001. p. 1139-54.
    • (2001) Disorders of Hemoglobin , pp. 1139-1154
    • Fucharoen, S.1
  • 6
    • 0031782419 scopus 로고    scopus 로고
    • Hemoglobin E. β-Thalassemia: An increasingly common disease with some diagnostic pitfalls
    • Weatherall DJ. Hemoglobin E. β-Thalassemia: an increasingly common disease with some diagnostic pitfalls. J Pediatr 1998;132:765-7.
    • (1998) J Pediatr , vol.132 , pp. 765-767
    • Weatherall, D.J.1
  • 7
    • 0034091983 scopus 로고    scopus 로고
    • Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions
    • Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol 2000;108:295-9.
    • (2000) Br J Haematol , vol.108 , pp. 295-299
    • Liu, Y.T.1    Old, J.M.2    Miles, K.3    Fisher, C.A.4    Weatherall, D.J.5    Clegg, J.B.6
  • 9
    • 0037305250 scopus 로고    scopus 로고
    • Hemoglobin H disease: Not necessarily a benign disorder
    • Chui DH, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood 2003;101:791-800.
    • (2003) Blood , vol.101 , pp. 791-800
    • Chui, D.H.1    Fucharoen, S.2    Chan, V.3
  • 10
    • 0025006416 scopus 로고
    • Detection of the hemoglobin E mutation using the color complementation assay: Application to complex genotyping
    • Embury SH, Kropp GL, Stanton TS, Warren TC, Cornett PA, Chehab FF. Detection of the hemoglobin E mutation using the color complementation assay: application to complex genotyping. Blood 1990;76:619-23.
    • (1990) Blood , vol.76 , pp. 619-623
    • Embury, S.H.1    Kropp, G.L.2    Stanton, T.S.3    Warren, T.C.4    Cornett, P.A.5    Chehab, F.F.6
  • 12
    • 0034321997 scopus 로고    scopus 로고
    • Genetic factors affecting clinical severity in beta-thalassemia syndromes
    • Winichagoon P, Fucharoen S, Chen P, Wasi P. Genetic factors affecting clinical severity in beta-thalassemia syndromes. J Pediatr Hematol Oncol 2000;22:573-80.
    • (2000) J Pediatr Hematol Oncol , vol.22 , pp. 573-580
    • Winichagoon, P.1    Fucharoen, S.2    Chen, P.3    Wasi, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.