Putative BCHE gene involvement in a reciprocal translocation t(3;5)(q26;q22) in an unusual myelogenous disorder with myeloproliferative and dysplastic features

被引:0
|
作者
Streubel, B
Füreder, W
Jordan, H
Walchshofer, S
Wimazal, F
Jäger, U
Geissler, K
Schwartz, L
Chott, A
Lechner, K
Valent, P
Fonatsch, C
机构
[1] Univ Vienna, Inst Med Biol, Vienna, Austria
[2] Univ Vienna, Div Hematol & Hemostaseol, Dept Internal Med 1, Vienna, Austria
[3] Virginia Commonwealth Univ, Dept Microbiol & Immunol, Richmond, VA USA
[4] Univ Vienna, Dept Clin Pathol, Vienna, Austria
来源
CYTOGENETICS AND CELL GENETICS | 1999年 / 85卷 / 1-2期
关键词
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P343
引用
收藏
页码:87 / 87
页数:1
相关论文
共 50 条
  • [41] 慢性粒细胞白血病急变伴t(3;21)(q26;q22)染色体易位受累基因的研究
    刘旭平
    张美荣
    代芸
    张莉
    李睿
    郝玉书
    肖志坚
    中华血液学杂志, 2006, (05) : 310 - 313
  • [42] Myeloid/natural killer cell blast crisis representing an additional translocation, t(3;7)(q26;q21) in Philadelphia-positive chronic myelogenous leukemia
    Henzan, H
    Yoshimoto, G
    Okeda, A
    Nagasaki, Y
    Hirano, G
    Takase, K
    Tanimoto, T
    Miyamoto, T
    Fukuda, T
    Nagafuji, K
    Harada, M
    ANNALS OF HEMATOLOGY, 2004, 83 (12) : 784 - 788
  • [43] Report of an unusual translocation t(3;14)(q26;q32) involving both EVI1 and IGH in an unclassified acute myeloid leukaemia (AML)
    Havelange, V.
    Ameye, G.
    Deweer, A.
    Bahloula, K.
    Mullier, C.
    Libouton, J. M.
    Detrait, M.
    Saussoys, P.
    Poppe, B.
    Speleman, F.
    Ferrant, A.
    Poirel, H. A.
    ACTA CLINICA BELGICA, 2007, 62 (04) : 254 - 254
  • [44] Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3
    Andreas Tzschach
    Maria Hoeltzenbein
    Kirsten Hoffmann
    Corinna Menzel
    Alexander Beyer
    Volker Ocker
    Goetz Wurster
    Martine Raynaud
    Hans-Hilger Ropers
    Vera Kalscheuer
    Helmut Heilbronner
    European Journal of Human Genetics, 2006, 14 : 1317 - 1320
  • [45] Heterotaxy and cardiac defect in a girl with chromosome translocation t(X; 1)(q26;p13.1) and involvement of ZIC3
    Tzschach, Andreas
    Hoeltzenbein, Maria
    Hoffmann, Kirsten
    Menzel, Corinna
    Beyer, Alexander
    Ocker, Volker
    Wurster, Goetz
    Raynaud, Martine
    Ropers, Hans-Hilger
    Kalscheuer, Vera
    Heilbronner, Helmut
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (12) : 1317 - 1320
  • [46] De novo balanced reciprocal translocation mosaic t(1;3)(q42;q25) detected by prenatal genetic diagnosis: a fetus conceived using preimplantation genetic testing due to a t(12;14)(q22;q13) balanced paternal reciprocal translocation
    Zhang, Shaoqin
    Zhu, Jianjiang
    Qi, Hong
    Xu, Limei
    Cai, Lirong
    Meng, Ran
    MOLECULAR CYTOGENETICS, 2021, 14 (01)
  • [47] De novo balanced reciprocal translocation mosaic t(1;3)(q42;q25) detected by prenatal genetic diagnosis: a fetus conceived using preimplantation genetic testing due to a t(12;14)(q22;q13) balanced paternal reciprocal translocation
    Shaoqin Zhang
    Jianjiang Zhu
    Hong Qi
    Limei Xu
    Lirong Cai
    Ran Meng
    Molecular Cytogenetics, 14
  • [48] A novel translocation t(3;21)(p21;q22) in acute myelogenous leukemia preceding a late-appearing Philadelphia chromosome
    A Quintás-Cardama
    L V Abruzzo
    F J Giles
    J Jorgensen
    J Cortes
    J E Sarriera
    H Kantarjian
    S Verstovsek
    Leukemia, 2006, 20 : 1638 - 1640
  • [49] A novel translocation t(3;21)(p21;q22) in acute myelogenous leukemia preceding a late-appearing Philadelphia chromosome
    Quintas-Cardama, A.
    Abruzzo, L. V.
    Giles, F. J.
    Jorgensen, J.
    Cortes, J.
    Sarriera, J. E.
    Kantarjian, H.
    Verstovsek, S.
    LEUKEMIA, 2006, 20 (09) : 1638 - 1640
  • [50] Prenatal finding of a fetus with 47,XX,t(4;5)(q26;p15),+der(4)t(4;5)mat due to familial balanced reciprocal translocation
    Zhao, Xiao Xi
    EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2010, 150 (01) : 104 - 106