The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations-Reference-Cited by-同舟云学术

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The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations

Published:2010-01-21 Issue:8 Volume:19 Page:1507-1514
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Paulsson K.,Haferlach C.,Fonatsch C.,Hagemeijer A.,Andersen M. K.,Slovak M. L.,Johansson B.,

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/19/8/1507/1529280/ddq024.pdf

Reference30 articles.

1. Chromosomal banding patterns in 88 cases of acute nonlymphocytic leukemia

2. Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia

3. Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?

4. Isodicentric X chromosome in a patient with myelodysplastic syndrome

5. Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphocytic leukemia

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1. Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia;Blood Cancer Journal;2020-05

2. A complex and cryptic intrachromosomal rearrangement generating the FIP1L1_PDGFRA in adult acute myeloid leukemia;Cancer Genetics;2019-11

3. Isolated isochromosomes i(X)(p10) and idic(X)(q13) are associated with myeloid malignancies and dysplastic features;American Journal of Hematology;2019-08-26

4. Pediatric acute myeloid leukemia with t(7;21)(p22;q22);Genes, Chromosomes and Cancer;2019-02-14

5.

Identification of chromosomal abnormalities and genomic features in near-triploidy/tetraploidy-acute leukemia by fluorescence in situ hybridization

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