Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia (Q59529485)

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scientific article published on 14 September 2006

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English	Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia	scientific article published on 14 September 2006

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scholarly article

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30 December 2019

Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia (English)

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30 December 2019

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lymphoblastic leukemia

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1

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30 December 2019

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30 December 2019

author name string

Heidenblad M

2

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30 December 2019

Mörse H

3

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30 December 2019

Borg A

4

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30 December 2019

Johansson B

6

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30 December 2019

publication date

14 September 2006

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30 December 2019

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20

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30 December 2019

11

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30 December 2019

2002-2007

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30 December 2019

Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia

1 reference

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Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia

1 reference

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Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling

1 reference

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Comparative expressed sequence hybridization studies of high-hyperdiploid childhood acute lymphoblastic leukemia.

1 reference

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Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.

1 reference

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Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis.

1 reference

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High frequency of leukemic clones in newborn screening blood samples of children with B-precursor acute lymphoblastic leukemia

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Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins.

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Identification of preleukemic precursors of hyperdiploid acute lymphoblastic leukemia in cord blood

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7 January 2021

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Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia

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7 January 2021

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Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.

1 reference

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7 January 2021

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FLT3 mutations in childhood acute lymphoblastic leukemia

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FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy

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Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis

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Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping

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Comparative genomic hybridization as part of a new diagnostic strategy in childhood hyperdiploid acute lymphoblastic leukemia.

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High-resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia.

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A tiling resolution DNA microarray with complete coverage of the human genome

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A set of BAC clones spanning the human genome

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Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis

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Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias

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7 January 2021

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High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

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Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation

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CGH-Plotter: MATLAB toolbox for CGH-data analysis

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BioArray Software Environment (BASE): a platform for comprehensive management and analysis of microarray data.

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Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: an interphase FISH analysis.

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Interphase molecular cytogenetic screening for chromosomal abnormalities of prognostic significance in childhood acute lymphoblastic leukaemia: a UK Cancer Cytogenetics Group Study.

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Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas

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Trisomy 4 Leading to Duplication of a Mutated KIT Allele in Acute Myeloid Leukemia with Mast Cell Involvement

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Identifiers

10.1038/SJ.LEU.2404372

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16990785%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16990785%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

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