(Q47366317)

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Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics

scientific article published in February 2004

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

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4

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Ulrich Germing

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

Brigitte Royer-Pokora

5

object named as

Brigitte Royer-Pokora

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

author name string

Detlef Trost

1

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

Barbara Hildebrandt

2

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

Nicola Müller

3

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

publication date

1 February 2004

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

Leukemia Research

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

28

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

2

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

171-177

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Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

The myelodysplastic syndrome(s): a perspective and review highlighting current controversies

1 reference

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Diagnostic and prognostic significance of cytogenetics in adult primary myelodysplastic syndromes

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7 January 2021

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

1 reference

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7 January 2021

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Chromosomal alterations associated with evolution from myelodysplastic syndrome to acute myeloid leukemia

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Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases

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Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map.

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Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome

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Physical mapping of the minimal region of loss in 5q- chromosome

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Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization

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Interphase fluorescence in situ hybridization overcomes pitfalls of G-banding analysis with special reference to underestimation of chromosomal aberration rates

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An optimized set of human telomere clones for studying telomere integrity and architecture.

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Genetic alterations in hormone-refractory recurrent prostate carcinomas

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Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization

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Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses. A study of 54 cases with hematological disorders

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Masked monosomy 7 in myelodysplastic syndromes is uncommon and of undetermined clinical significance

1 reference

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7 January 2021

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Primary myelodysplastic syndrome with normal cytogenetics: utility of 'FISH panel testing' and M-FISH.

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7 January 2021

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Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2803%2900221-2

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Clinical importance of interphase cytogenetics detecting occult chromosome lesions in myelodysplastic syndromes with normal karyotype

1 reference

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Identifiers

10.1016/S0145-2126(03)00221-2

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/14654082

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