(Q57690149)

A Zagaria

3

0 references

Luisa Anelli

L Anelli

2

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Pietro D'Addabbo

P D'Addabbo

5

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Francesco Albano

F Albano

1

0 references

Mariano Rocchi

M Rocchi

7

0 references

Giorgina Specchia

G Specchia

8

0 references

author name string

V Liso

“Home-brew” FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia

6

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language of work or name

English

0 references

publication date

25 January 2010

0 references

published in

Oncogene

0 references

volume

29

0 references

issue

17

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page(s)

2509-2516

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Primate segmental duplications: crucibles of evolution, diversity and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Segmental duplications and evolutionary plasticity at tumor chromosome break-prone regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Double-strand breaks and translocations in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Mechanisms for human genomic rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Quantitative PCR identifies a minimal deleted region of 120 kb extending from the Philadelphia chromosome ABL translocation breakpoint in chronic myeloid leukemia with poor outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Evolutionary-new centromeres preferentially emerge within gene deserts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Duplication hotspots, rare genomic disorders, and common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Heterogeneous prognostic impact of derivative chromosome 9 deletions in chronic myelogenous leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524

Clinical implications of der(9q) deletions detected through dual-fusion fluorescence in situ hybridization in patients with chronic myeloid leukemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2009.524