Array CGH analysis reveals deletion of chromosome 22q11 in CLL with normal karyotype and no fish alterations

被引：1
|
作者：
Mestichelli, Francesca [1 ]
Dalsass, Alessia [1 ]
Ferretti, Silvia [1 ]
Camaioni, Elisa [1 ]
Angelini, Mario [1 ]
Mei, Sabrina [1 ]
Pezzoni, Valerio [1 ]
Travaglini, Fosco [1 ]
Troiani, Emanuela [1 ]
Angelini, Stefano [1 ]
Galieni, Piero [1 ]
机构：
[1] Osped CG Mazzoni, UOC Ematol, Ascoli Piceno, Italy
来源：
BRITISH JOURNAL OF HAEMATOLOGY | 2018年 / 183卷 / 01期
关键词：
array CGH; chronic lymphocytic leukaemia; loss of 22q11; CHRONIC LYMPHOCYTIC-LEUKEMIA; COMPARATIVE GENOMIC HYBRIDIZATION; PRAME GENE; CYTOGENETICS; ABERRATIONS; EXPRESSION;
D O I：
10.1111/bjh.14949
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：152 / 155
页数：4
相关论文
共 50 条
  • [21] TETRALOGY OF FALLOT ASSOCIATED WITH CHROMOSOME 22Q11 DELETION
    MOMMA, K
    KONDO, C
    ANDO, M
    MATSUOKA, R
    TAKAO, A
    AMERICAN JOURNAL OF CARDIOLOGY, 1995, 76 (08): : 618 - &
  • [22] Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene
    Gunn, Shelly R.
    Bolla, Aswani R.
    Barron, Lynn L.
    Gorre, Mercedes E.
    Mohammed, Mansoor S.
    Bahler, David W.
    Mellink, Clemens H. M.
    van Oers, Marinus H. J.
    Keating, Michael J.
    Ferrajoli, Alessandra
    Coombes, Kevin R.
    Abruzzo, Lynne V.
    Robetorye, Ryan S.
    LEUKEMIA RESEARCH, 2009, 33 (09) : 1276 - 1281
  • [23] Application of ultra-high resolution fine-tiling array CGH (FT-CGH) to the analysis of 22q11 deletion syndrome
    Urban, A
    Selzer, R
    Richmond, T
    Popescu, G
    Cubells, JF
    Green, R
    Emanuel, B
    Weissman, SM
    Snyder, M
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 138B (01) : 138 - 138
  • [24] Truncus arteriosus communis associated with chromosome 22q11 deletion
    Momma, K
    Ando, M
    Matsuoka, R
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (04) : 1067 - 1071
  • [25] Vasomotor instability in neonates with chromosome 22q11 deletion syndrome
    Shashi, V
    Berry, MN
    Hines, MH
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 121A (03) : 231 - 234
  • [26] Deletion in chromosome region 22q11 in a child with CHARGE association
    Devriendt, K
    Swillen, A
    Fryns, JP
    CLINICAL GENETICS, 1998, 53 (05) : 408 - 410
  • [27] Anesthetic management of a child with chromosome 22q11 deletion syndrome
    Yotsui-Tsuchimochi, H
    Higa, K
    Matsunaga, M
    Nitahara, K
    Shono, S
    PEDIATRIC ANESTHESIA, 2006, 16 (04) : 454 - 457
  • [28] Cortical dysgenesis in 2 patients with chromosome 22q11 deletion
    Bird, LM
    Scambler, P
    CLINICAL GENETICS, 2000, 58 (01) : 64 - 68
  • [29] An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman
    Toutain, Jerome
    Taine, Laurence
    Morice-Picard, Fanny
    Hallal, Houria
    Dai, Zong-Qi
    Arveiler, Benoit
    Lacombe, Didier
    Horovitz, Jacques
    Saura, Robert
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2011, 54 (03) : 292 - 294
  • [30] High-density oligonucleotide tiling array based Very-High Resolution CGH and its application to the analysis of breakpoints in Chromosome 22Q and in 22Q11 Deletion Syndrome
    Urban, Alexander Eckehart
    Korbel, Jan
    Grubert, Fabian
    Selzer, Rebecca
    Richmond, Todd
    Hacker, April
    Green, Roland
    Emanuel, Beverly S.
    Gerstein, Mark
    Weissman, Sherman M.
    Snyder, Michael
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (07) : 698 - 698
12345