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Volumn 69, Issue 2, 1997, Pages 263-267

Rare β-thalassemia mutation in a Turkish patient: FSC-36/37 (-T)

Author keywords

ORIGIN OF MUTATION; RARE MUTATIONS; TURKEY; THALASSEMIA

Indexed keywords


EID: 1842366684     PISSN: 00187143     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (8)

References (16)
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  • 2
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  • 3
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    • Molecular characterization of β-thalassemia in Azerbaijan
    • Çuruk, M.A., G.T. Yuregir, C.D. Asadov et al. 1992. Molecular characterization of β-thalassemia in Azerbaijan. Hum. Genet. 90:417-419.
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    • Çuruk, M.A.1    Yuregir, G.T.2    Asadov, C.D.3
  • 4
    • 0023863374 scopus 로고
    • The detection of β-globin gene mutations in β-thalassemia using oligonucleotide probes and amplified DNA
    • Diaz-Chico, J.C., K.G. Yang, G.D. Efremov et al. 1988. The detection of β-globin gene mutations in β-thalassemia using oligonucleotide probes and amplified DNA. Biochim. Biophys. Acta 949:43-48.
    • (1988) Biochim. Biophys. Acta , vol.949 , pp. 43-48
    • Diaz-Chico, J.C.1    Yang, K.G.2    Efremov, G.D.3
  • 5
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  • 6
    • 0028026865 scopus 로고
    • Two rare mutations [Cd 30 (G-C) and Cds 36/37 (-T)] in a Turkish thalassemia major patient from Bulgaria
    • Jankovic, L., D. Plaseska, G.D. Efremov et al. 1994. Two rare mutations [Cd 30 (G-C) and Cds 36/37 (-T)] in a Turkish thalassemia major patient from Bulgaria. Hemoglobin 18:359-364.
    • (1994) Hemoglobin , vol.18 , pp. 359-364
    • Jankovic, L.1    Plaseska, D.2    Efremov, G.D.3
  • 7
    • 0025296040 scopus 로고
    • The thalassemia syndromes: Molecular basis and prenatal diagnosis in 1990
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    • (1990) Sem. Hematol. , vol.27 , pp. 209-228
    • Kazazian Jr., H.H.1
  • 8
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  • 10
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    • Poncz, M.1    Solowiejczky, D.2    Harpel, B.3
  • 11
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  • 12
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.