Is idic(X)(q13) a Myelodysplasia-Defining Genetic Alteration in MDS and AML?

被引：0
|
作者：
Hu, Aileen [1 ]
Zhang, Ling [2 ]
Gao, Juehua [3 ]
Wu, Xiaojun [4 ]
Zheng, Gang [5 ]
Shao, Lina [6 ]
Quesada, Andres [1 ]
Wang, Endi [7 ]
Cui, Wei [8 ]
Tang, Guilin [1 ]
Xu, Xinjie [5 ]
Zou, Ying [9 ]
Lu, Xinyan [10 ]
Song, Jinming [2 ]
Wang, Xiaoqiong [11 ]
Patel, Keyur [1 ]
Medeiros, L. Jeffrey [1 ]
Hu, Shimin [1 ]
机构：
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[3] Northwestern Mem Hosp, Chicago, IL USA
[4] Johns Hopkins Sch Med, Baltimore, MD USA
[5] Mayo Clin, Rochester, MN USA
[6] Univ Michigan, Ann Arbor, MI USA
[7] Univ Southern Calif, Keck Sch Med USC, Los Angeles, CA USA
[8] Univ Kansas, Med Ctr, Kansas City, KS USA
[9] Johns Hopkins Univ, Baltimore, MA USA
[10] Northwestern Univ, Feinberg Sch Med, Chicago, IL USA
[11] Univ Miami, Miami, FL USA
来源：
LABORATORY INVESTIGATION | 2024年 / 104卷 / 03期
关键词：
D O I：
暂无
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
1136
引用
收藏
页码：S1414 / S1415
页数：2
相关论文
共 50 条
  • [11] Translocation (12;17)(q13;q23) in de novo acute myeloid leukemia with trilineage myelodysplasia
    Wong, KF
    So, CC
    Yu, PH
    CANCER GENETICS AND CYTOGENETICS, 1999, 114 (02) : 159 - 161
  • [12] Translocation (X;5)(q13;q33) in essential thrombocythemia
    Munro, LR
    Stevenson, DAJ
    Culligan, DJ
    CANCER GENETICS AND CYTOGENETICS, 1999, 114 (01) : 78 - 79
  • [13] A case of myelodysplasia syndrome with an unusual 46,XY,t(20;22)(q13;q11.2) karyotype.
    Sinha, M
    Macera, MJ
    Mizhiritskaya, V
    Zeng, R
    Babu, A
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 225 - 225
  • [14] GENETIC IMBALANCES IN MYELODYSPLASTIC SYNDROMES(MDS) AND ACUTE MYELOID LEUKEMIA (AML) PATIENTS WITH CHROMOSOME 11Q13 ABNORMALITIES
    Bernasconi, P.
    Dambruoso, I.
    Boni, M.
    Zappatore, R.
    Cavigliano, P. M.
    Giardini, I.
    Caresana, M.
    Tarantino, P.
    Invernizzi, R.
    Lazzarino, M.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 : 273 - 274
  • [15] Translocation (X;20)(q13;q13.3): Report of three additional cases
    Sreekantaiah, Chandrika
    BLOOD, 2007, 110 (11) : 134B - 134B
  • [16] Infant t(1;22)(p13;q13)AML-M7: A real entity for the WHO AML classification.
    Duchayne, E
    Fenneteau, O
    Pages, MP
    Sainty, D
    Arnoulet, C
    Dastugue, N
    Garand, R
    Flandrin, G
    BLOOD, 2001, 98 (11) : 581A - 581A
  • [17] ISODICENTRIC (X)(Q13) - A NEW CHARACTERISTIC CHROMOSOMAL ANOMALY IN MYELOPROLIFERATIVE SYNDROME
    PETIT, P
    FRYNS, JP
    MASURE, R
    VANDENBERGHE, H
    CANCER GENETICS AND CYTOGENETICS, 1982, 7 (04) : 339 - 341
  • [18] Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits
    Smith, M
    Woodroffe, A
    Smith, R
    Holguin, S
    Martinez, J
    Filipek, PA
    Modahl, C
    Moore, B
    Bocian, ME
    Mays, L
    Laulhere, T
    Flodman, P
    Spence, MA
    CYTOGENETIC AND GENOME RESEARCH, 2002, 98 (04) : 233 - 239
  • [19] The t(X;20)(q13;q13) translocation is a good prognostic factor in myeloid neoplasms: A report of 25 cases from the Groupe Francophone de Cytogenetique Hematologique
    Nguyen-Khac, Florence
    Muller, Marc
    Chapiro, Elise
    Abermil, Nassera
    Collonge-Rame, Marie-Agnes
    Daudignon, Agnes
    Gaillard, Baptiste
    Guzun, Doina
    Ittel, Antoine
    Lefebvre, Christine
    Lesesve, Jean-Francois
    Mozziconacci, Marie-Joelle
    Penther, Dominique
    Quessada, Julie
    Settegrana, Catherine
    Smagghe, Luce
    Terre, Christine
    Veronese, Lauren
    Hirsch, Pierre
    Troadec, Marie-Berengere
    AMERICAN JOURNAL OF HEMATOLOGY, 2024, 99 (07) : 1420 - 1422
  • [20] 45,X/46,X r(X)(p22.2∷q13)一例
    宋洁
    王英
    韩彦龙
    中华医学遗传学杂志, 2005, (01) : 115 - 115
12345