Array CGH analysis reveals deletion of chromosome 22q11 in CLL with normal karyotype and no fish alterations
Author:
Affiliation:
1. U.O.C Ematologia, Ospedale C.G. Mazzoni; Ascoli Piceno Italy
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14949/fullpdf
Reference10 articles.
1. Immunostimulatory oligonucleotide-induced metaphase cytogenetics detect chromosomal aberrations in 80% of CLL patients: a study of 132 CLL cases with correlation to FISH, IgVH status, and CD38 expression;Dicker;Blood,2006
2. Genomic aberrations and survival in chronic lymphocytic leukemia;Döhner;New England Journal of Medicine,2000
3. Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia;Gunn;The Journal of Molecular Diagnostics: JMD,2008
4. Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene;Gunn;Leukemia Research,2009
5. Clinical application of array based comparative genomic hybridization for the identification of prognostically important genetic alterations in chronic lymphocytic leukemia;Higgins;Molecular Diagnosis and Therapy,2008
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Detection of a deletion at 22q11 locus involvingZNF280A/ZNF280B/PRAME/GGTLC2in B‐cell malignancies: simply a consequence of an immunoglobulin lambda light chain rearrangement;British Journal of Haematology;2019-04-15
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