IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL. (Q27851563)

2

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V H J van der Velden

3

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S V van Reijmersdal

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R Venkatachalam

5

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B Scheijen

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E Sonneveld

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J J M van Dongen

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A J P Veerman

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F N van Leeuwen

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A Geurts van Kessel

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P M Hoogerbrugge

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

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publication date

July 2010

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published in

Leukemia

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volume

24

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issue

7

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page(s)

1258-64

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Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia

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BCR–ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros

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Acute lymphoblastic leukemia

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Detailed clonality analysis of relapsing precursor B acute lymphoblastic leukemia: implications for minimal residual disease detection

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Relapse in children with acute lymphoblastic leukemia involving selection of a preexisting drug-resistant subclone

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Precursor-B-ALL with D(H)-J(H) gene rearrangements have an immature immunogenotype with a high frequency of oligoclonality and hyperdiploidy of chromosome 14

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Application of germline IGH probes in real-time quantitative PCR for the detection of minimal residual disease in acute lymphoblastic leukemia

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Comparative analysis of T-cell receptor gene rearrangements at diagnosis and relapse of T-cell acute lymphoblastic leukemia (T-ALL) shows high stability of clonal markers for monitoring of minimal residual disease and reveals the occurrence of secon

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JAK mutations in high-risk childhood acute lymphoblastic leukemia

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7 January 2021

Identifiers

DOI

10.1038/LEU.2010.87

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

2387662

1044642798

0 references

2387662

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference