TrianglePUBLICATIONS · 28063196
ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
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Bibliographic metadata only. No full-text article or abstract is reproduced. Absence of a captured notice is not confirmation that a publication is clear of corrections or retractions.
- Journal
- Genes Chromosomes Cancer
- Publication date
- 2017 May
- First author
- Yamato G
Publication notices
- absence is not clearance
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- false
- has expression of concern metadata
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- relationships
Authors and identifiers
- name
- Yamato G
- type
- Author
- name
- Shiba N
- type
- Author
- name
- Yoshida K
- type
- Author
- name
- Shiraishi Y
- type
- Author
- name
- Hara Y
- type
- Author
- name
- Ohki K
- type
- Author
- name
- Okubo J
- type
- Author
- name
- Okuno H
- type
- Author
- name
- Chiba K
- type
- Author
- name
- Tanaka H
- type
- Author
- name
- Kinoshita A
- type
- Author
- name
- Moritake H
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Yamato G
- type
- Author
- name
- Shiba N
- type
- Author
- name
- Yoshida K
- type
- Author
- name
- Shiraishi Y
- type
- Author
- name
- Hara Y
- type
- Author
- name
- Ohki K
- type
- Author
- name
- Okubo J
- type
- Author
- name
- Okuno H
- type
- Author
- name
- Chiba K
- type
- Author
- name
- Tanaka H
- type
- Author
- name
- Kinoshita A
- type
- Author
- name
- Moritake H
- type
- Author
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- book metadata
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- document type
- citation
- dois
- 10.1002/gcc.22443
- electronic publication date
- display
- 2017 Feb 14
- precision
- day
- year
- 2017
- evidence scope
- bibliographic_metadata_only
- id
- pubmed:28063196
- immutable id
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- journal
- abbreviation
- Genes Chromosomes Cancer
- issn electronic
- 1098-2264
- issn print
- 1045-2257
- issue
- 5
- name
- Genes, chromosomes & cancer
- nlm unique id
- 9007329
- pages
- 382-393
- volume
- 56
- languages
- eng
- notices
- absence is not clearance
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- retrieved at
- 2026-09-09T23:47:23.138359+00:00
- publication date
- display
- 2017 May
- precision
- month
- year
- 2017
- publication types
- Journal Article
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
Preserved source evidence · Independent clinical review pending · Not medical advice