DELETION OF 14Q INVOLVING IGH GENE IN PATIENTS WITH MULTIPLE MYELOMA

被引:0
|
作者
Balcarkova, J. [1 ]
Pika, T. [1 ]
Urbankova, H. [1 ]
Holzerova, M. [1 ]
Scudla, V. [1 ]
Bacovky, J. [1 ]
Indrak, K. [1 ]
Jarosova, M. [1 ]
机构
[1] Univ Hosp Olomouc, Olomouc, Czech Republic
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2009年 / 94卷
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
0062
引用
收藏
页码:25 / 25
页数:1
相关论文
共 50 条
  • [21] Interstitial del(14)(Q) involving IGH are recurrent in MM
    Pospisilova, H.
    Baens, M.
    Michaux, L.
    Stul, M.
    Van Hummelen, P.
    Van Loo, P.
    Vermeesch, J.
    Jarosova, M.
    Zemanova, Z.
    Michalova, K.
    Van den Berghe, I.
    Alexander, H. D.
    Maes, B.
    Franke, S.
    Hagemeijer, A.
    denberghe, P.
    Cools, J.
    De Wolf-Peeters, C.
    Marynen, P.
    Wlodarska, I.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2007, 92 (06): : 101 - 101
  • [22] Concerning "14q(22) deletion in a familial case of anophthalmia with polydactyly"
    Velagaleti, GVN
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 126A (01) : 108 - 108
  • [23] The characterisation and isolation of translocations involving the IGH locus in multiple myeloma
    Fenton, JAL
    Proffitt, JA
    Pratt, G
    Rawstron, AC
    Davies, FE
    Morgan, GJ
    BRITISH JOURNAL OF CANCER, 1998, 78 : 57 - 57
  • [24] Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation
    Bagci, Gulseren
    Cetin, Gokhan Ozan
    Semerci, Nur
    Toruner, Gokce A.
    Cinbis, Mine
    CLINICAL DYSMORPHOLOGY, 2012, 21 (01) : 37 - 41
  • [25] Detection of unusual IGH breakpoints in t(11;14) (q13;q32) multiple myeloma
    Trakhtenbrot, Luba
    Stanevsky, Anfisa
    Nagler, Arnon
    Amariglio, Ninette
    CHROMOSOME RESEARCH, 2011, 19 : S178 - S179
  • [26] Inherited 14q Duplication and 21q Deletion: A Rare Adjacent-2 Segregation in Multiple Family Members
    Dave, Bhavana J.
    Olney, Ann Haskins
    Zaleski, Dianna H.
    Pickering, Diane L.
    Becker, Troy A.
    Chipman, Hope E.
    Sanger, Warren G.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (10) : 2248 - 2253
  • [27] A case of terminal 14q deletion with de novo unbalanced t(Y;14)(q?;q32) translocation
    Bagci, G.
    Cetin, G.
    Semerci, C.
    Toruner, G.
    Cinbis, M.
    CHROMOSOME RESEARCH, 2009, 17 : 66 - 66
  • [28] Identification of 13q deletion, trisomy 1q, and IgH rearrangement as the most frequent chromosomal changes found in Korean patients with multiple myeloma
    Bang, Soo-Mee
    Kim, Young Ree
    Cho, Han Ik
    Chi, Hyun Sook
    Seo, Eul-Ju
    Park, Chan Jeoung
    Yoo, Soo Jin
    Kim, Hee Chan
    Chun, Hong Gu
    Min, Hyun Chung
    Oh, Bo Ra
    Kim, Tae Young
    Lee, Jae Hoon
    Lee, Dong Soon
    CANCER GENETICS AND CYTOGENETICS, 2006, 168 (02) : 124 - 132
  • [29] Neoplastic circulating endothelial cells in multiple myeloma with 13q14 deletion
    Rigolin, GM
    Fraulini, C
    Ciccone, M
    Mauro, E
    Bugli, AM
    De Angeli, C
    Negrini, M
    Cuneo, A
    Castoldi, G
    BLOOD, 2006, 107 (06) : 2531 - 2535
  • [30] 14q terminal deletion:: Prenatal diagnosis in a child with severe congenital anomalies
    Mertens, DJLM
    De Die-Smulders, CEM
    Kampschöer, PHNM
    Offermans, JPM
    Engelen, JJM
    Hamers, AJH
    Lammens, M
    Schrander-Stumpel, CTRM
    GENETIC COUNSELING, 2000, 11 (04): : 341 - 346