(Q38485684)

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Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study

scientific article published on January 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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Kajsa Paulsson

1

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Thoas Fioretos

2

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author name string

Bodil Strömbeck

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Nils Mauritzson

4

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Europe PubMed Central

PubMed publication ID

3 September 2017

Hans J Tanke

5

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Europe PubMed Central

PubMed publication ID

3 September 2017

Bertil Johansson

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

1 January 2003

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Europe PubMed Central

PubMed publication ID

3 September 2017

Cancer Genetics and Cytogenetics

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Europe PubMed Central

PubMed publication ID

3 September 2017

140

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Europe PubMed Central

PubMed publication ID

3 September 2017

1

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Europe PubMed Central

PubMed publication ID

3 September 2017

66-69

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Europe PubMed Central

PubMed publication ID

3 September 2017

A single-center population-based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender

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

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The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology

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Involvement and functional impairment of the CD34(+)CD38(-)Thy-1(+) hematopoietic stem cell pool in myelodysplastic syndromes with trisomy 8.

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New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling

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A study to determine whether trisomy 8, deleted 9q and trisomy 22 are markers of cryptic rearrangements of PML/RARalpha, AML1/ETO and CBFB/MYH11 respectively in acute myeloid leukaemia. MRC Adult Leukaemia Working Party. Medical Research Council

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

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Spectral karyotyping and multicolor fluorescence in situ hybridization reveal new tumor-specific chromosomal aberrations

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Comparison of spectral karyotyping and conventional cytogenetics in 39 patients with acute myeloid leukemia and myelodysplastic syndrome

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Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2

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Acute leukemia cytogenetics: an evaluation of combining G-band karyotyping with multi-color spectral karyotyping

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Subtle chromosomal rearrangements in children with unexplained mental retardation

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Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL)

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A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay

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A case of inv(8)(p11q24) associated with acute myeloid leukemia involves the MOZ and CBP genes in a masked t(8;16)

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Fluorescence In Situ Hybridization Analysis of Masked (8;21)(q22;q22) Translocations

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c-myc locus amplification and the acquisition of trisomy 8 in the evolution of chronic myeloid leukaemia

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Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics

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Identifiers

10.1016/S0165-4608(02)00628-3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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