Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations (Q81381430)

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8 January 2020

title

Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations (English)

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8 January 2020

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1 reference

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8 January 2020

Griffiths M

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8 January 2020

Mason J

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8 January 2020

Rindl M

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8 January 2020

Akiki S

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8 January 2020

McMullan D

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8 January 2020

Stinton V

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8 January 2020

Powell H

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8 January 2020

Curtis A

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8 January 2020

Bown N

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8 January 2020

publication date

1 December 2005

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8 January 2020

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8 January 2020

volume

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8 January 2020

issue

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8 January 2020

page(s)

2355-2358

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The role of FLT3 in haematopoietic malignancies

8 January 2020

cites work

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7 January 2021

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group

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7 January 2021

The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the Unite

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7 January 2021

Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis

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7 January 2021

Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease

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7 January 2021

Genomic structure of human FLT3: implications for mutational analysis

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7 January 2021

Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis.

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7 January 2021