메뉴 건너뛰기




Volumn 74, Issue 4, 1997, Pages 199-201

Primary acquired sideroblastic anemia, thrombocytosis, and trisomy 8

Author keywords

Myelodysplasia; Thrombocytosis; Trisomy 8

Indexed keywords

AGED; ARTICLE; CASE REPORT; CELL LINEAGE; CHROMOSOME 3; CHROMOSOME 5; HUMAN; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; SIDEROBLASTIC ANEMIA; THROMBOCYTE COUNT; THROMBOCYTOSIS; TRISOMY 8;

EID: 0030965120     PISSN: 09395555     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002770050283     Document Type: Article
Times cited : (10)

References (8)
  • 1
    • 0016348695 scopus 로고
    • Distinct haematological disorder with the deletion of the long arm of no. 5 chromosome
    • Van Den Berghe H, Cassiman JJ, David G, et al (1974) Distinct haematological disorder with the deletion of the long arm of no. 5 chromosome. Nature 251: 437-438
    • (1974) Nature , vol.251 , pp. 437-438
    • Van Den Berghe, H.1    Cassiman, J.J.2    David, G.3
  • 2
    • 0028026968 scopus 로고
    • Correlation of cytogenetic findings with clinical features in 18 patients with inversion (3) (q21;q26) or t(3;3) (q21;q26)
    • Fontasch C, Gudart H, Lengfelder E, et al (1994) Correlation of cytogenetic findings with clinical features in 18 patients with inversion (3) (q21;q26) or t(3;3) (q21;q26). Leukemia 8:1318-1326
    • (1994) Leukemia , vol.8 , pp. 1318-1326
    • Fontasch, C.1    Gudart, H.2    Lengfelder, E.3
  • 3
    • 0022448249 scopus 로고
    • Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes
    • Yunis JJ, Rydell RE, Oken MM, et al (1986) Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes. Blood 67:1721-1730
    • (1986) Blood , vol.67 , pp. 1721-1730
    • Yunis, J.J.1    Rydell, R.E.2    Oken, M.M.3
  • 4
    • 0016725149 scopus 로고
    • A new haematological syndrome with distinct karyotype: The 5q- Syndrome
    • Sokal G, Michaux JL, Van Den Berghe H, et al (1975) A new haematological syndrome with distinct karyotype: the 5q-syndrome. Blood 46:519-528
    • (1975) Blood , vol.46 , pp. 519-528
    • Sokal, G.1    Michaux, J.L.2    Van Den Berghe, H.3
  • 5
    • 0022383747 scopus 로고
    • Rearrangements of chromosome 3 involving band 3q21 and 3q26 are associated with normal or elevated platelet counts in acute nonlymphoblastic leukaemia
    • Bitter MA, Neilly ME, Le Beau MM , Pearson MG, Rowley JD (1985) Rearrangements of chromosome 3 involving band 3q21 and 3q26 are associated with normal or elevated platelet counts in acute nonlymphoblastic leukaemia. Blood 66:1362-1370
    • (1985) Blood , vol.66 , pp. 1362-1370
    • Bitter, M.A.1    Neilly, M.E.2    Le Beau, M.M.3    Pearson, M.G.4    Rowley, J.D.5
  • 6
    • 0021205863 scopus 로고
    • A new translocation t(1:3) (p36:q21) in myelodysplastic disorders
    • Moir DJ, Jones PAE, Duncan JR, Cook P, Buckle VJ (1984) A new translocation t(1:3) (p36:q21) in myelodysplastic disorders. Blood 64:553-555
    • (1984) Blood , vol.64 , pp. 553-555
    • Moir, D.J.1    Jones, P.A.E.2    Duncan, J.R.3    Cook, P.4    Buckle, V.J.5
  • 7
    • 0024469383 scopus 로고
    • Cytogenetics and their prognostic value in de novo acute myeloid leukaemia: A report on 283 cases
    • Fenaux P, Preudhomme C, Lai JL, et al (1989) Cytogenetics and their prognostic value in de novo acute myeloid leukaemia: a report on 283 cases. Br J Haematol 73:61-67
    • (1989) Br J Haematol , vol.73 , pp. 61-67
    • Fenaux, P.1    Preudhomme, C.2    Lai, J.L.3
  • 8
    • 0029866001 scopus 로고    scopus 로고
    • Molecular and cytogenetic abnormalities in acute myeloid leukaemia and myelodysplastic syndromes
    • De Greef GE , Hagemeijer A (1996) Molecular and cytogenetic abnormalities in acute myeloid leukaemia and myelodysplastic syndromes. Baillieres Clin Haematol 9:1-18
    • (1996) Baillieres Clin Haematol , vol.9 , pp. 1-18
    • De Greef, G.E.1    Hagemeijer, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.