Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference7 articles.
1. MLL rearangements in haematological malignancies: lessons from clinical and biological studies;DiMartino;Br J Haematol,1999
2. Cryptic t(4;11) encoding MLL-AF4 due to insertion of 5′ MLL sequences in chromosome 4;von Bergh;Leukemia,2001
3. Molecular analysis of the genomic inversion and insertion of AF10 into MLL suggests a single-step event;Chaplin;Genes Chromosomes Cancer,2001
4. An ins(X;11)(q24;q23) fuses the MLL and the Septin 6/K1AA0128 gene in an infant with AML-M2;Borkhardt;Genes Chromosomes Cancer,2001
5. Two acute monocytic leukemia (AML-M5a) cell lines (MOLM-13 and MOLM-14) with interclonal phenotypic heterogeneity showing MLL-AF9 fusion resulting from an occult chromosome insertion, ins(11;9)(q23;p22p23);Matsuo;Leukemia,1997
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1. Recurrent Cytogenetic Abnormalities in Acute Myeloid Leukemia;Methods in Molecular Biology;2016-12-02
2. The heterogeneity of pediatric MLL-rearranged acute myeloid leukemia;Leukemia;2011-05-13
3. 5′ MLL Gene Deletion in a Case with Childhood Acute Lymphoblastic Leukemia;Laboratory Medicine;2010-02
4. MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literature;Cancer Genetics and Cytogenetics;2008-05
5. Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case;Cancer Genetics and Cytogenetics;2007-04
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