Novel Chromosome 16 Abnormality—der(16)del(16)(q13)t(16;21)(p11.2;q22)—Associated with Acute Myeloid Leukemia-Reference-Cited by-同舟云学术

Novel Chromosome 16 Abnormality—der(16)del(16)(q13)t(16;21)(p11.2;q22)—Associated with Acute Myeloid Leukemia

Published:1999-08 Issue:1 Volume:113 Page:25-28
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Sharma P.,Watson N.,Robson L.,Gallo J.,Smith A.

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference17 articles.

1. Partial deletion of the long arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia;Arthur;Blood,1983

2. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia;LeBeau;N Engl J Med,1983

3. Acute non-lymphocytic leukemia with t(16;21);Nobbs;Cancer Genet Cytogenet,1993

4. Establishment of a novel human acute myeloblastic leukemia cell line (YNH-1) with t(16;21),t(1;16) and 12q13 translocations;Yamamoto;Leukemia,1997

5. Consistent detection of TLS/FUS-ERG chimeric transcripts in acute myeloid leukemia with t(16;21)(p11;q22) and identification of a novel transcript;Kong;Blood,1997

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1. TLS/FUS-ERG fusion gene in acute leukemia and myelodysplastic syndrome evolved to acute leukemia: report of six cases and a literature review;Annals of Hematology;2022-10-01

2. Adult B-cell acute lymphoblastic leukemia with two unrelated abnormal cytogenetic clones;Cancer Genetics and Cytogenetics;2010-08

3. A novel cytogenetic abnormality in Burkitt lymphoma associated with treatment resistant disease;Clinical and Laboratory Haematology;2005-10

4. Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16;Genome Research;2005-09

5. Deletion of 16q11 is a recurrent cytogenetic aberration in acute myeloblastic leukemia during disease progression;Cancer Genetics and Cytogenetics;2001-11