Fluorescence in situ hybridization (FISH) reveals unexpected cryptic chromosome 11 defects in MDS/AML patients.

被引:0
|
作者
Bernasconi, Paolo [1 ]
Dambruoso, Irene [1 ]
Boni, Marina [1 ]
Cavigliano, Paola Maria [1 ]
Giardini, Ilaria [1 ]
Zappatore, Rita [1 ]
Calatroni, Silvia [1 ]
Rocca, Barbara [1 ]
Caresana, Marilena [1 ]
Lazzarino, Mario [1 ]
机构
[1] Fdn Policlin San Mateo, IRCCS, Div Hematol, Pavia, Italy
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
4413
引用
收藏
页码:181B / 181B
页数:1
相关论文
共 50 条
  • [41] Assessment of chromosome 1 imbalance in neoplasms and fibrocystic disease of the breast by fluorescence in situ hybridization (FISH).
    Kattar, MM
    Wallis, T
    Visscher, DW
    MODERN PATHOLOGY, 1998, 11 (01) : 22A - 22A
  • [42] Assessment of chromosome 1 imbalance in neoplasms and fibrocystic disease of the breast by fluorescence in situ hybridization (FISH).
    Kattar, MM
    Wallis, T
    Visscher, DW
    LABORATORY INVESTIGATION, 1998, 78 (01) : 22A - 22A
  • [43] Physical organization of repetitive sequences and chromosome diversity of barley revealed by fluorescence in situ hybridization (FISH)
    Zhang, Siyu
    Zhu, Minqiu
    Shang, Yi
    Wang, Jiaqi
    Dawadundup
    Zhuang, Lifang
    Zhang, Jinlong
    Chu, Chenggen
    Qi, Zengjun
    GENOME, 2019, 62 (05) : 329 - 339
  • [44] Physical mapping by multi colour FISH of translocations accompanied by deletions of chromosome 22 in MDS patients.
    Sinclair, P
    Green, AR
    Nacheva, E
    JOURNAL OF MEDICAL GENETICS, 1997, 34 : 245 - 245
  • [45] Interphase analysis of chromosome 11 in human pituitary somatotroph adenomas by direct fluorescence in situ hybridization
    Kontogeorgos, G
    Kapranos, N
    ENDOCRINE PATHOLOGY, 1996, 7 (03) : 203 - 206
  • [46] INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-11 DETERMINED BY FLUORESCENCE IN-SITU HYBRIDIZATION
    HORI, T
    MASUNO, M
    WAKAZONO, A
    TAKAHASHI, E
    KATAKURA, R
    ORII, T
    JAPANESE JOURNAL OF HUMAN GENETICS, 1993, 38 (02): : 219 - 224
  • [47] High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration
    K Paulsson
    M Heidenblad
    B Strömbeck
    J Staaf
    G Jönsson
    Å Borg
    T Fioretos
    B Johansson
    Leukemia, 2006, 20 : 840 - 846
  • [48] High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration
    Paulsson, K
    Heidenblad, M
    Strömbeck, B
    Staaf, J
    Jönsson, G
    Fioretos, T
    Johansson, B
    LEUKEMIA, 2006, 20 (05) : 840 - 846
  • [49] Clinical comparison of variable number tandem repeats (VNTR), and fluorescence in situ hybridization (FISH) in allogeneic stem cell transplant patients.
    Abella, E
    KuKurga, D
    Du, W
    Mohamed, A
    Bakdounes, K
    Nadeau, T
    Karanes, C
    Klein, J
    Dansey, R
    Cassells, L
    Peters, W
    Baynes, R
    BLOOD, 1998, 92 (10) : 135A - 135A
  • [50] Chromosomal abnormalities identified by fluorescence in situ hybridization (FISH) in semi-solid cultured progenitors from myelodysplastic syndrome patients.
    Dupont, JM
    Fichelson, S
    FontenayRoupie, M
    LeTessier, D
    Rabineau, D
    Dreyfus, F
    BLOOD, 1996, 88 (10) : 3343 - 3343