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双色间期荧光原位杂交对隐匿性t(15;17)急性早幼粒细胞白血病的诊断价值 被引量:2

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出处 《中华内科杂志》 CAS CSCD 北大核心 2003年第7期509-510,共2页 Chinese Journal of Internal Medicine
基金 江苏省自然科学基金资助项目 (BK199915 3 ) 苏州市科技局资助项目 (ZS0 2 0 1)
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  • 1李玉蓉,安红艳,吕环,张彩霞.46,XX,t(2;15)携带者二例[J].中国优生与遗传杂志,2004,12(4):136-136. 被引量:1
  • 2肖冰,李建勇,潘金兰,马力,仇海荣,吴亚芳,薛永权.多重荧光原位杂交检测骨髓增生异常综合征患者复杂核型异常[J].中华血液学杂志,2005,26(9):513-516. 被引量:12
  • 3Grignani F, Fagioli M. Alcalay M, et al. Acute promyelocytic leukemia: from genetics to treatment. Blood. 1994; 83 : 10 -25
  • 4de-la Chapelle A, Knuutila S, Elonen E, et al. Chromosomal abnormalities in acute promyelocytic leukaemia. Stand J Haematol, 1981 ;26:57 - 60
  • 5Shaffer LG, Tommerup N. An International System for Human Cytogenetic Nomenclature. Basel: ISCN. 2005 : 1 - 130
  • 6Schoch C, Haase D, Haferlach T, et al. Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t( 15 ;17 ) ( q22;q21 ) : a report on 50 patients. Br J Haematol, 1996 ;94:493 - 500
  • 7Berger R, Le Coniat M, Derre J, et al. Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities. Genes Chromosomes Cancer, 1991 ;3:332 - 337
  • 8Johansson B, Mertens F, Mitelman F, et al. Secondary chromosomal abnormalities in acute leukemias. Leukemia, 1994;8 : 953 - 962
  • 9Xu L, Zhao WL, Xiong SM, et al. Molecular cytogenetic characterization and clinical relevance of additonnal,complex and/or variant chromosome abnormalites in acule promyelocytic leukemia. Leukemia ,2001 ;15:1359 - 1368
  • 10Chou WC, Tang JL, Yao M, et al. Clinical and biological characteristics of acute promyelocytic leukemia in Taiwan: a high relapse rate in patients with high initial and peak white blood cell counts during all-trans retinoic acid treatment. Leukemia, 1997;11:921 - 928

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