Dic(17;18)(p11.2;p11.2) Is a Recurring Abnormality in Chronic Lymphocytic Leukemia Associated with Aggressive Disease

被引：4
|
作者：
Woyach, Jennifer A. [1 ]
Byrd, John C. [1 ]
Zhao, John [1 ]
McFaddin, Andrew [1 ]
Ruppert, Amy S. [1 ]
Lin, Thomas S. [2 ]
Andritsos, Leslie [1 ]
Blum, Kristie A. [1 ]
Flynn, Joseph M. [1 ]
Jones, Jeffrey Alan [1 ]
Heerema, Nyla A. [1 ]
机构：
[1] Ohio State Univ, Columbus, OH 43210 USA
[2] GlaxoSmithKline Inc, Collegeville, PA USA
来源：
BLOOD | 2009年 / 114卷 / 22期
关键词：
D O I：
10.1182/blood.V114.22.539.539
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：508 / 508
页数：1
相关论文
共 50 条
  • [1] Dic(17;18)(p11.2;p11.2) is a recurring abnormality in chronic lymphocytic leukaemia associated with aggressive disease
    Woyach, Jennifer A.
    Heerema, Nyla A.
    Zhao, John
    McFaddin, Andrew
    Stark, Amy
    Lin, Thomas S.
    Andritsos, Leslie A.
    Blum, Kristie A.
    Flynn, Joseph M.
    Jones, Jeffrey A.
    Byrd, John C.
    BRITISH JOURNAL OF HAEMATOLOGY, 2010, 148 (05) : 754 - 759
  • [2] Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2)
    Mikhail, Fady M.
    McIlvried, Dawn
    Holt, R. Lynn
    Messiaen, Ludwine
    Descartes, Maria D.
    Carroll, Andrew J.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (15) : 1647 - 1654
  • [3] Behavioral characterization of mouse models for Smith-Magenis syndrome and Dup 17 (p11.2 p11.2)
    Walz, K
    Spencer, C
    Kaasik, K
    Lee, CC
    Lupski, JR
    Paylor, R
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 519 - 519
  • [4] Familial deletion of chromosome 18 (p11.2)
    Velagaleti, GVN
    Harris, S
    Carpenter, NJ
    Coldwell, J
    Say, B
    ANNALES DE GENETIQUE, 1996, 39 (04): : 201 - 204
  • [5] Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies
    Tirado, Carlos A.
    Meloni-Ehrig, Aurelia M.
    Wallenhorst, Eian
    Burks, Kristine
    Scheerle, Jay
    Morillon, Maurice
    Kelly, JoAnn C.
    Heritage, Deborah
    Spira, Alexander
    Croft, Calvin D.
    Glasser, Lewis
    Butera, James N.
    Mowrey, Philip
    CANCER GENETICS AND CYTOGENETICS, 2006, 170 (01) : 61 - 64
  • [6] Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11)
    Smith, A
    Das, P
    O'Reilly, J
    Patsouris, C
    Campbell, LJ
    CANCER GENETICS AND CYTOGENETICS, 2006, 166 (01) : 86 - 88
  • [7] 5 CASES DEMONSTRATING THE DISTINCTIVE BEHAVIORAL FEATURES OF CHROMOSOME DELETION 17(P11.2 P11.2) (SMITH-MAGENIS SYNDROME)
    COLLEY, AF
    LEVERSHA, MA
    VOULLAIRE, LE
    ROGERS, JG
    JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 1990, 26 (01) : 17 - 21
  • [8] Synovial sarcoma of the prostate with t(X;18)(p11.2;q11.2)
    Iwasaki, H
    Ishiguro, M
    Ohjimi, Y
    Ikegami, H
    Takeuchi, T
    Kikuchi, M
    Kaneko, Y
    Ariyoshi, A
    AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1999, 23 (02) : 220 - 226
  • [9] A rare der(10)t(X;10)(p11.2;p11.2) in an elderly patient with therapy-related acute myelomonocytic leukemia
    Manabe, Masahiro
    Tanizawa, Nao
    Nanno, Satoru
    Hagiwara, Yuuji
    Asada, Reiko
    Koh, Ki-Ryang
    EJHAEM, 2022, 3 (01): : 256 - 258
  • [10] INTERSTITIAL DELETION OF (17)(P11.2) - A MICRODELETION SYNDROME - ANOTHER EXAMPLE
    DEALMEIDA, JCC
    REIS, DF
    MARTINS, RR
    ANNALES DE GENETIQUE, 1989, 32 (03): : 184 - 186
12345