DIAGNOSIS OF T(11-14)(Q13-Q32) USING INTERPHASE FLUORESCENT IN-SITU HYBRIDIZATION

被引：0
|
作者：
LEROUX, D [1 ]
MONTEIL, M [1 ]
机构：
[1] UNIV J FOURIER,FAC MED GRENOBLE,DEPT GENET,F-38706 LA TRONCHE,FRANCE
来源：
BLOOD | 1994年 / 84卷 / 10期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：A608 / A608
页数：1
相关论文
共 50 条
  • [21] Diagnosis of mantle cell lymphoma by detection of t(11;14)(q13;q32) by fluorescence in situ hybridization in peripheral blood and bone marrow specimens
    Remstein, ED
    Hanson, CA
    Dewald, GW
    LABORATORY INVESTIGATION, 2002, 82 (01) : 261A - 261A
  • [22] Diagnosis of mantle cell lymphoma by detection of t(11;14)(q13;q32) by fluorescence in situ hybridization in peripheral blood and bone marrow specimens
    Remstein, ED
    Hanson, CA
    Dewald, GW
    MODERN PATHOLOGY, 2002, 15 (01) : 261A - 261A
  • [23] Application of interphase cytogenetics for the detection of t(11;14)(q13;q32) in mantle cell lymphomas
    Siebert, R
    Matthiesen, P
    Harder, S
    Zhang, Y
    Borowski, A
    Zuhlke-Jenisch, R
    Plendl, H
    Metzke, S
    Joos, S
    Zucca, E
    Weber-Matthiesen, K
    Roggero, E
    Grote, W
    Schlegelberger, B
    ANNALS OF ONCOLOGY, 1998, 9 (05) : 519 - 526
  • [24] Automated fluorescent in situ hybridization (FISH) analysis of t(9;22)(q34;q11) in interphase nuclei
    Kajtar, Bela
    Mehes, Gabor
    Loerch, Thomas
    Deak, Linda
    Kneifne, Marika
    Alpar, Donat
    Pajor, Laszlo
    CYTOMETRY PART A, 2006, 69A (06) : 506 - 514
  • [25] PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 1Q USING FLUORESCENT IN-SITU HYBRIDIZATION
    DUPONT, BR
    HUFF, RW
    RIDGWAY, LE
    STRATTON, RF
    MOORE, CM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 50 (01): : 21 - 27
  • [26] CHARACTERIZATION OF A NEW NON-HODGKINS LYMPHOMA CELL-LINE (NCEB-1) WITH A CHROMOSOMAL (11-14) TRANSLOCATION [T(11-14)(Q13 - Q32)]
    SALTMAN, DL
    CACHIA, PG
    DEWAR, AE
    ROSS, FM
    KRAJEWSKI, AS
    LUDLAM, C
    STEEL, CM
    BLOOD, 1988, 72 (06) : 2026 - 2030
  • [27] MOLECULAR ANALYSIS OF THE T(11-14) (Q13-Q32) TRANSLOCATION ASSOCIATED WITH LYMPHOCYTIC-B LEUKEMIA AND LYMPHOMA - CHROMOSOME-11 BREAKPOINTS SPAN AT LEAST 63 KILOBASES OF THE BCL-1 LOCUS
    MEEKER, T
    CLINICAL RESEARCH, 1991, 39 (01): : A32 - A32
  • [28] INTERSTITIAL DUPLICATION AND TRIPLICATION OF 15Q11-Q13 CONFIRMED BY FLUORESCENCE IN-SITU HYBRIDIZATION
    CRAWFORD, EC
    LETHCO, BA
    BEALER, D
    SCHROER, RJ
    CLARKSON, KB
    PHELAN, MC
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 618 - 618
  • [29] Genetics of t(11;14)(q13;q32)-negative MCL
    Wlodarska, I.
    Vanhentenrijk, V.
    Pospisilova, H.
    Van Roosbroeck, K.
    Stul, M.
    Francesca, M.
    Dierickx, D.
    Verhoef, G.
    Vandenberghe, P.
    Dewolf-Peeters, C.
    ACTA CLINICA BELGICA, 2007, 62 (04) : 259 - 259
  • [30] Derivative (14)t(11;14)(q13;q32)t(11;14)(p11.2;p11.2): a novel unbalanced variant of the t(11;14)(q13;q32) translocation in mantle cell lymphoma
    Sathanoori, Malini
    Shekhter-Levin, Sofia
    Marks, Stanley M.
    Swerdlow, Steven H.
    CANCER GENETICS AND CYTOGENETICS, 2007, 172 (02) : 158 - 164
12345