A COMPLEX KARYOTYPE INCLUDING A TRANSLOCATION T(1;12)(Q21;P13) IN A CASE OF HIGH-RISK MYELODYSPLASTIC SYNDROME

被引：0
|
作者：
Sun, W. [1 ]
Jia, R. [1 ]
Liu, C. [1 ]
Li, H. [2 ,3 ]
Zhao, H. [1 ]
Wan, S. [1 ]
Su, L. [1 ]
机构：
[1] Capital Med Univ, Xuanwu Hosp, Dept Hematol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Hematol, Beijing 100730, Peoples R China
[3] Peking Union Med Coll, Beijing 100021, Peoples R China
来源：
LEUKEMIA RESEARCH | 2015年 / 39卷
关键词：
D O I：
10.1016/S0145-2126(15)30197-1
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
196
引用
收藏
页码：S98 / S98
页数：1
相关论文
共 50 条
  • [31] Concurrent Waldenstrom's Macroglobulinemia and Myelodysplastic Syndrome with a Sequent t(10;13)(p13;q22) Translocation
    DeRosa, Peter A.
    Roche, Kyle C.
    Nava, Victor E.
    Singh, Sunita
    Liu, Min-Ling
    Agarwal, Anita
    CURRENT ONCOLOGY, 2022, 29 (07) : 4587 - 4592
  • [32] Three-Way Translocation t(12;15;17) (p13;q24;q21) Found in Acute Promyelocytic Leukemia with Basophilic Differentiation
    Frazzetto, Sara
    Gullo, Lara
    Sapuppo, Gabriele
    Fazio, Manlio
    Lo Faro, Cristina
    Giunta, Giuliana
    Caravotta, Ignazio
    Mauro, Elisa
    Parisi, Marina Silvia
    Triolo, Anna Maria
    Parrinello, Nunziatina Laura
    Consoli, Maria Letizia
    Tambe, Loredana
    Cambria, Daniela
    Marino, Sara
    Scuderi, Grazia
    Di Raimondo, Francesco
    HEMATOLOGY REPORTS, 2024, 16 (02) : 367 - 374
  • [33] Role of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13)
    Janssen, Hilde
    Wlodarska, Iwona
    Mecucci, Cristina
    Hagemeijer, Anne
    Vandenberghe, Peter
    Marynen, Peter
    Cools, Jan
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2006, 91 (07): : 949 - 951
  • [34] Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation
    Petit, P
    Devriendt, K
    Vermeesch, JR
    De Cock, P
    Fryns, JP
    ANNALES DE GENETIQUE, 1998, 41 (01): : 22 - 26
  • [35] MOLECULAR CYTOGENETIC ANALYSES OF 12P13.3 JARID1A GENE IN A CASE OF MYELODYSPALSTIC SYNDROME WITH A COMPLEX T(12;21)(P13;Q22)
    Buijs, A.
    Dekker, A. W.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 : 517 - 517
  • [36] Myelodysplastic syndrome with translocation (1;12)(p36;p13) and rearrangement of TEL-ETV6.
    Helias, C
    Ferrant, D
    Goasguen, JE
    Ly-Sunnaram, B
    Jego, P
    Busson-Le Coniat, M
    Berger, R
    Lessard, M
    BLOOD, 1999, 94 (10) : 284B - 284B
  • [37] Mukoepidermoidkarzinom der SpeicheldrüseUngewöhnliche Varianten mit Nachweis der Translokation t(11,19)(q21;p13)Salivary gland mucoepidermoid carcinomaUnusual variants with detection of the t(11,19)(q21;p13) translocation
    S. Schwarz
    C. Stiegler
    J. Zenk
    H. Iro
    A. Agaimy
    Der Pathologe, 2009, 30 (6): : 472 - 477
  • [38] AN ATYPICAL FAMILIAL T(15, 21)(P13, Q22) TRANSLOCATION RESULTING IN DOWN SYNDROME
    VINSON, PC
    HOWARDPEEBLES, PN
    SMITH, JL
    FINLEY, WH
    FINLEY, SC
    CLINICAL RESEARCH, 1980, 28 (05): : A859 - A859
  • [39] Germline MYOF1::WNK4 and VPS25::MYOF1 Chimeras Generated by the Constitutional Translocation t(17;19)(q21;p13) in Two Siblings With Myelodysplastic Syndrome
    Panagopoulos, Ioannis
    Andersen, Kristin
    Stavseth, Vidar
    Torkildsen, Synne
    Heim, Sverre
    Tandsaether, Maren randi
    CANCER GENOMICS & PROTEOMICS, 2024, 21 (03) : 272 - 284
  • [40] Molecular cytogenetics of t(12;21)(p13;q22)
    Bernard, OA
    Romana, SP
    Poirel, H
    Berger, R
    LEUKEMIA & LYMPHOMA, 1996, 23 (5-6) : 459 - &
12345