메뉴 건너뛰기




Volumn 13, Issue 4, 2011, Pages 369-370

A multiplex approach to the molecular diagnosis of β-thalassemia

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN; BETA GLOBULIN;

EID: 80054063050     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmoldx.2011.05.001     Document Type: Note
Times cited : (2)

References (6)
  • 1
    • 77953952024 scopus 로고    scopus 로고
    • The inherited diseases of hemoglobin are an emerging global health burden
    • Weatherall DJ: The inherited diseases of hemoglobin are an emerging global health burden. Blood 2010, 115:4331-4336
    • (2010) Blood , vol.115 , pp. 4331-4336
    • Weatherall, D.J.1
  • 2
    • 0033983971 scopus 로고    scopus 로고
    • Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia
    • January 1
    • Chong SS, Boehm CD, Higgs DR, Cutting, GR: Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood 2000, 95; January 1:360-362
    • (2000) Blood , vol.95 , pp. 360-362
    • Chong, S.S.1    Boehm, C.D.2    Higgs, D.R.3    Cutting, G.R.4
  • 3
    • 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
    • DOI 10.1136/jmg.2005.033597
    • Harteveld CL, Voskamp A, Phylipsen M, Akkermans N, den Dunnen JT, White SJ, Giordano PC: 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, 42:922-931 (Pubitemid 41811314)
    • (2005) Journal of Medical Genetics , vol.42 , Issue.12 , pp. 922-931
    • Harteveld, C.L.1    Voskamp, A.2    Phylipsen, M.3    Akkermans, N.4    Den, D.J.T.5    White, S.J.6    Giordano, P.C.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.