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Volumn 59, Issue 1, 1998, Pages 15-21

Genetic and hematological studies in a group of 114 adult patients with SC sickle cell disease

Author keywords

Alpha thalassemia; Beta globin gene haplotypes; SC sickle cell disease

Indexed keywords

BETA GLOBIN;

EID: 0031855763     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199809)59:1<15::AID-AJH4>3.0.CO;2-2     Document Type: Article
Times cited : (17)

References (27)
  • 1
    • 0025825869 scopus 로고
    • The distinct pathobiology of sickle cell-hemoglobin C disease
    • Nagel RL, Lawrence C: The distinct pathobiology of sickle cell-hemoglobin C disease. Hematol-Oncol Clin N Am 5:433-451, 1991.
    • (1991) Hematol-Oncol Clin N Am , vol.5 , pp. 433-451
    • Nagel, R.L.1    Lawrence, C.2
  • 4
    • 0026691572 scopus 로고
    • A PCR-based strategy to detect the common severe determinants of α thalassaemia
    • Bowden DK, Vickers MA, Higgs DR: A PCR-based strategy to detect the common severe determinants of α thalassaemia. Br J Haematol 81:104-108, 1992.
    • (1992) Br J Haematol , vol.81 , pp. 104-108
    • Bowden, D.K.1    Vickers, M.A.2    Higgs, D.R.3
  • 5
    • 0024376665 scopus 로고
    • Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes
    • Sutton M, Bouhassira EE, Nagel RL: Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes. Am J Hematol 32:66-69, 1989.
    • (1989) Am J Hematol , vol.32 , pp. 66-69
    • Sutton, M.1    Bouhassira, E.E.2    Nagel, R.L.3
  • 6
    • 0018888252 scopus 로고
    • Inaccuracies associated with the automated measurement of mean cell hemoglobin concentration in dehydrated cells
    • Mohandas N, Clark MR, Kissinger S, Bayer C, and Shohet SB: Inaccuracies associated with the automated measurement of mean cell hemoglobin concentration in dehydrated cells. Blood 56:125-128, 1980.
    • (1980) Blood , vol.56 , pp. 125-128
    • Mohandas, N.1    Clark, M.R.2    Kissinger, S.3    Bayer, C.4    Shohet, S.B.5
  • 7
    • 0022543618 scopus 로고
    • Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser light scattering
    • Mohandas N, Kim YR, Tycko DH, Orlik J, Wyatt J, and Groner W: Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser light scattering. Blood 68:506-513, 1986.
    • (1986) Blood , vol.68 , pp. 506-513
    • Mohandas, N.1    Kim, Y.R.2    Tycko, D.H.3    Orlik, J.4    Wyatt, J.5    Groner, W.6
  • 8
    • 0023877789 scopus 로고
    • Erythrocytes in Hb SC disease are microcytic and hyperchromic
    • Ballas SK, Kocher W: Erythrocytes in Hb SC disease are microcytic and hyperchromic. Am J Hematol 28:37-39, 1988.
    • (1988) Am J Hematol , vol.28 , pp. 37-39
    • Ballas, S.K.1    Kocher, W.2
  • 10
    • 0024360719 scopus 로고
    • β-cluster haplotypes, α-gene status, and hematological data from SS, SC, and S-β-thalassemia patients in Southern California
    • Schroeder WA, Powars DR, Kay LM, Chan LS, Van Huynh, Shelton JB, Shelton JR: β-cluster haplotypes, α-gene status, and hematological data from SS, SC, and S-β-thalassemia patients in Southern California. Hemoglobin 13:325-353, 1989.
    • (1989) Hemoglobin , vol.13 , pp. 325-353
    • Schroeder, W.A.1    Powars, D.R.2    Kay, L.M.3    Chan, L.S.4    Van Huynh5    Shelton, J.B.6    Shelton, J.R.7
  • 14
    • 0022588206 scopus 로고
    • Association of the level of Gγ chain in the fetal hemoglobin of normal adults with specific haplotypes
    • Hattori Y, Kutlar F, Mosley CJ, Mayson SM, Huisman THJ: Association of the level of Gγ chain in the fetal hemoglobin of normal adults with specific haplotypes. Hemoglobin 10:185-204, 1986.
    • (1986) Hemoglobin , vol.10 , pp. 185-204
    • Hattori, Y.1    Kutlar, F.2    Mosley, C.J.3    Mayson, S.M.4    Huisman, T.H.J.5
  • 17
    • 0025109527 scopus 로고
    • The variable expression of sickle cell disease is genetically determined
    • Powars D, Chan LS, Schroeder WA: The variable expression of sickle cell disease is genetically determined. Semin Hematol 27:360-376, 1990.
    • (1990) Semin Hematol , vol.27 , pp. 360-376
    • Powars, D.1    Chan, L.S.2    Schroeder, W.A.3
  • 20
    • 0026708201 scopus 로고
    • Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2
    • Dover GJ, Smith KD, Chang YC, Purvis S, Mays A, Meyers DA, Sheils C, Serjeant G: Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. Blood 80:816-824, 1992.
    • (1992) Blood , vol.80 , pp. 816-824
    • Dover, G.J.1    Smith, K.D.2    Chang, Y.C.3    Purvis, S.4    Mays, A.5    Meyers, D.A.6    Sheils, C.7    Serjeant, G.8
  • 22
    • 0029670772 scopus 로고    scopus 로고
    • βs haplotypes, α-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I)
    • Kéclard L, Ollendorf V, Berchel C, Loret H, and Mérault G: βs haplotypes, α-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I). Hemoglobin 20:63-74, 1996.
    • (1996) Hemoglobin , vol.20 , pp. 63-74
    • Kéclard, L.1    Ollendorf, V.2    Berchel, C.3    Loret, H.4    Mérault, G.5
  • 23
    • 0002792420 scopus 로고
    • Genetic modulators of disease
    • Embury SH, Hebbel RP, Mohandas N, Steinberg MH, eds. New York: Raven Press
    • Embury SH, Steinberg MH: Genetic modulators of disease. In Embury SH, Hebbel RP, Mohandas N, Steinberg MH, eds. Sickle Cell Disease: Basic Principles and Clinical Practice. New York: Raven Press, 1994, pp 279-298.
    • (1994) Sickle Cell Disease: Basic Principles and Clinical Practice , pp. 279-298
    • Embury, S.H.1    Steinberg, M.H.2
  • 27
    • 0025963843 scopus 로고
    • Effect of β-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia
    • Rieder RF, Safaya S, Gillette P, Fryd S, Hsu H, Adams JG, III, Steinberg MH: Effect of β-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia. Am J Hematol 36:184-189, 1991.
    • (1991) Am J Hematol , vol.36 , pp. 184-189
    • Rieder, R.F.1    Safaya, S.2    Gillette, P.3    Fryd, S.4    Hsu, H.5    Adams III, J.G.6    Steinberg, M.H.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.