(Q44003370)

English

Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: report from an international workshop

scientific article published in April 2002

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 November 2017

Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: report from an international workshop (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

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acute myeloid leukemia

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Krzysztof Mrózek

4

object named as

Krzysztof Mrózek

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Europe PubMed Central

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28 November 2017

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object named as

Janet D Rowley

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28 November 2017

author name string

Harold J Olney

1

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Europe PubMed Central

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28 November 2017

Felix Mitelman

2

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28 November 2017

Bertil Johansson

3

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28 November 2017

Roland Berger

5

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Europe PubMed Central

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28 November 2017

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publication date

1 April 2002

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Europe PubMed Central

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28 November 2017

Genes, Chromosomes and Cancer

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Europe PubMed Central

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28 November 2017

33

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28 November 2017

4

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28 November 2017

413-423

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28 November 2017

The clinical significance of karyotype in acute myelogenous leukemia.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Preliminary data on the in vitro proliferation pattern and karyotypic characteristics in cells of patients with ANLL.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Subtle abnormalities in the short arm of chromosome 11 in acute myeloid leukemia.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Consistent interstitial chromosomal deletions in myeloid malignancies and their correlation with fragile sites

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Clinical importance of cytogenetics in acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Hematologic, clinical, and cytogenetic analysis in 109 patients with primary myelodysplastic syndrome. Prognostic significance of morphology and chromosome findings

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Therapy-related myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

21 January 2018

Trisomy 11 in myelodysplastic syndrome-derived acute myeloblastic leukaemias

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

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Translocation (2;3)(p22;q28) is associated with myeloid disorders

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Fourth International Workshop on Chromosomes in Leukemia 1982: Clinical significance of chromosomal abnormalities in acute nonlymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Hematologic manifestations associated with deletions of the long arm of chromosome 20

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

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An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

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Favorable cytogenetic abnormalities in secondary leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

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Chromosome abnormalities and karyotypic evolution in 83 patients with myelodysplastic syndrome and predictive value for prognosis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Cytogenetic polyclonality in hematologic malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Therapy-related leukemia and myelodysplastic syndrome: clinical, cytogenetic, and prognostic features

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

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Data management and statistical methods used in the analysis of balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and therapy-related acute leukemia: report from an international workshop

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Cytogenetic and fluorescence in situ hybridization analyses of hematologic malignancies in Korea

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Chromosome 16q, eosinophilia, and leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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Clinical and cytogenetic significance of myelodysplastic syndromes with disease evolution

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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International workshop on the relationship of prior therapy to balanced chromosome aberrations in therapy-related myelodysplastic syndromes and acute leukemia: overview report

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

inferred from DOI database lookup

3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

based on heuristic

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dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10045

7 January 2021

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10.1002/GCC.10045

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

release_4h4nnezg5zc2lpa5oqgsysf524

1 reference

https://api.fatcat.wiki/v0/release/4h4nnezg5zc2lpa5oqgsysf524

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

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