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Volumn 531, Issue , 2003, Pages 47-56

Alpha thalassaemia in Indonesia: Phenotypes and molecular defects

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; HEMOGLOBIN; HEMOGLOBIN A2; HEMOGLOBIN F; HEMOGLOBIN H; UNCLASSIFIED DRUG;

EID: 0042886064     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4615-0059-9_4     Document Type: Conference Paper
Times cited : (23)

References (21)
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    • Chang, J-G., Lee, L-S., Lin, C-P., and Chen, P-H., 1992, Rapid diagnosis of α-thalassemia-1 of Southeast Asia type and hydrops fetalis by polymerase chain reaction. Int. J. Hematol. 56: 155-159.
    • (1992) Int. J. Hematol. , vol.56 , pp. 155-159
    • Chang, J.-G.1    Lee, L.-S.2    Lin, C.-P.3    Chen, P.-H.4
  • 3
    • 0032055871 scopus 로고    scopus 로고
    • Hydrops fetalis caused by α- thalassaemia: An emerging health care problem
    • Chui, D.H.K., and Waye, J.S., 1998, Hydrops fetalis caused by α- thalassaemia: an emerging health care problem. Blood 91: 2213-2222.
    • (1998) Blood , vol.91 , pp. 2213-2222
    • Chui, D.H.K.1    Waye, J.S.2
  • 6
    • 0023112573 scopus 로고
    • Haemoglobinopathies in Southeast Asia
    • Fucharoen, S., and Winichagoon, P., 1987, Haemoglobinopathies in Southeast Asia. Haemoglobin 11: 65-88.
    • (1987) Haemoglobin , vol.11 , pp. 65-88
    • Fucharoen, S.1    Winichagoon, P.2
  • 7
    • 0027308859 scopus 로고
    • α-thalassemia
    • The Haemoglobinopathies (D.R. Higgs and D. Weatherall, eds.), W.B. Saunders, London
    • Higgs, D.R., 1993, α-thalassemia. In The Haemoglobinopathies (D.R. Higgs and D. Weatherall, eds.), Baillieres Clinical Haematology, W.B. Saunders, London, pp. 117-124.
    • (1993) Baillieres Clinical Haematology , pp. 117-124
    • Higgs, D.R.1
  • 8
    • 0021770859 scopus 로고
    • Independent recombination events between duplicated human ≈-globin genes: Implication for their concerted evolution
    • Higgs, D.R., Hill, A.V.S., Bowden, D.K., Weatherall, D.J., and Clegg, J.B., 1984, Independent recombination events between duplicated human ≈-globin genes: Implication for their concerted evolution. Nucleic Acid Res. 12: 6965-6977.
    • (1984) Nucleic Acid Res. , vol.12 , pp. 6965-6977
    • Higgs, D.R.1    Hill, A.V.S.2    Bowden, D.K.3    Weatherall, D.J.4    Clegg, J.B.5
  • 11
    • 0041872028 scopus 로고
    • Haemoglobin of newborn infants in Indonesia
    • Lie-Injo, L.E., 1959, Haemoglobin of newborn infants in Indonesia. Nature 183: 1125-1126.
    • (1959) Nature , vol.183 , pp. 1125-1126
    • Lie-Injo, L.E.1
  • 12
    • 0004912639 scopus 로고
    • Alpha chain thalassaemia and hydrops fetalis in Malaya, Report of five cases
    • Lie-Injo, LE., 1962, Alpha chain thalassaemia and hydrops fetalis in Malaya, Report of five cases. Blood 20: 581
    • (1962) Blood , vol.20 , pp. 581
    • Lie-Injo, L.E.1
  • 13
    • 0004910677 scopus 로고
    • Hydrops foetalis with a fast-moving haemoglobin
    • Lie-Injo, L.E., and Hie, J.B., 1960, Hydrops foetalis with a fast-moving haemoglobin. Br. Med. J. 2: 1649.
    • (1960) Br. Med. J. , vol.2 , pp. 1649
    • Lie-Injo, L.E.1    Hie, J.B.2
  • 15
    • 0042373031 scopus 로고
    • Gene deletions in alpha thalassemia prove that the 5′ zeta locus is functional
    • Pressley, L., Higgs, D.R., Clegg, J.B., and Weatherall, D.J., 1980, Gene deletions in alpha thalassemia prove that the 5′ zeta locus is functional. Proc. Natl. Acad. Sci. USA 77: 3386-3389.
    • (1980) Proc. Natl. Acad. Sci. USA , vol.77 , pp. 3386-3389
    • Pressley, L.1    Higgs, D.R.2    Clegg, J.B.3    Weatherall, D.J.4
  • 16
    • 0031834389 scopus 로고    scopus 로고
    • Molecular basis of β- thalassaemia in Indonesia: Application to prenatal deiagnosis
    • Setianingsih, I., Williamson, R., Marzuki, S., Harahap, A., Tamam, M., and Forrest, S., 1998, Molecular basis of β- thalassaemia in Indonesia: application to prenatal deiagnosis. Mol. Diag. 3: 11-20.
    • (1998) Mol. Diag. , vol.3 , pp. 11-20
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  • 19
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    • Interaction of an α-thalassaemia deletion with either a highly unstable α-globin variant (α2, codon 59, GGC→GAC) or a nondeletional α-thalassemia mutation (AATAAA→AATAAG): comparison of phenotypes illustrating "dominant" α- thalassaemia
    • Traeger-Synodinos, J., Metaxotou-Mavrommati, A., Karagiorga, M., Vrettou, C., Papassotiriou, I., Stamoulakatou, A., and Kanavakis, E., 1999, Interaction of an α-thalassaemia deletion with either a highly unstable α-globin variant (α2, codon 59, GGC→GAC) or a nondeletional α-thalassemia mutation (AATAAA→AATAAG): comparison of phenotypes illustrating "dominant" α- thalassaemia. Haemoglobin 23: 325-337.
    • (1999) Haemoglobin , vol.23 , pp. 325-337
    • Traeger-Synodinos, J.1    Metaxotou-Mavrommati, A.2    Karagiorga, M.3    Vrettou, C.4    Papassotiriou, I.5    Stamoulakatou, A.6    Kanavakis, E.7
  • 20
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.