Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q. (Q38489443)

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scientific article published on June 2002

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English	Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.	scientific article published on June 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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1 reference

based on heuristic

inferred from title

acute myeloid leukemia

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based on heuristic

inferred from title

Clara D. Bloomfield

4

object named as

Clara D Bloomfield

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Krzysztof Mrózek

1

object named as

Krzysztof Mrózek

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Kristiina Heinonen

2

object named as

Kristiina Heinonen

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

author name string

Karl S Theil

3

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Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

1 June 2002

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Europe PubMed Central

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3 September 2017

Genes, Chromosomes and Cancer

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Europe PubMed Central

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3 September 2017

34

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Europe PubMed Central

PubMed publication ID

3 September 2017

2

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Europe PubMed Central

PubMed publication ID

3 September 2017

137-153

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3 September 2017

Establishment and characterization of a megakaryoblast cell line with amplification of MLL.

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https://api.crossref.org/works/10.1002%2FGCC.10027

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.10027

21 January 2018

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

1 reference

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21 January 2018

The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Multicolor spectral karyotyping identifies novel translocations in childhood acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Clinical importance of cytogenetics in acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

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t(12;21): a new recurrent translocation in acute lymphoblastic leukemia.

1 reference

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Isodicentric chromosome 21: a novel aberration in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Twenty-four-color spectral karyotyping reveals chromosome aberrations in cytogenetically normal acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

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Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis

1 reference

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Fluorescence in situ hybridization analyses of hematologic malignancies reveal frequent cytogenetically unrecognized 12p rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

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Amplification of the 11q23 region in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

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MLL amplification in acute leukaemia: a United Kingdom Cancer Cytogenetics Group (UKCCG) study

1 reference

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21 January 2018

Novel translocation (2;4) with consistent involvement of 2p23 in acute nonlymphocytic leukemia (M2)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Increased karyotype precision using fluorescence in situ hybridization and spectral karyotyping in patients with myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

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

1 reference

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21 January 2018

Chromosomal differences between acute nonlymphocytic leukemia in patients with prior solid tumors and prior hematologic malignancies. A study of 14 cases with prior breast cancer

1 reference

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21 January 2018

MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10027

21 January 2018

Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysplastic syndrome

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Identifiers

10.1002/GCC.10027

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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