PUBLICATIONS · 29540347
RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior 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
- Blood
- Publication date
- 2018 May 17
- First author
- Yamato G
Publication notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
- false
- has retraction in link
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- pubmed marks article retracted
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- pubmed marks retraction notice
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- relationships
Authors and identifiers
- name
- Yamato G
- type
- Author
- name
- Shiba N
- type
- Author
- name
- Yoshida K
- type
- Author
- name
- Hara Y
- type
- Author
- name
- Shiraishi Y
- type
- Author
- name
- Ohki K
- type
- Author
- name
- Okubo J
- type
- Author
- name
- Park MJ
- type
- Author
- name
- Sotomatsu M
- type
- Author
- name
- Arakawa H
- type
- Author
- name
- Kiyokawa N
- type
- Author
- name
- Tomizawa D
- 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
- Hara Y
- type
- Author
- name
- Shiraishi Y
- type
- Author
- name
- Ohki K
- type
- Author
- name
- Okubo J
- type
- Author
- name
- Park MJ
- type
- Author
- name
- Sotomatsu M
- type
- Author
- name
- Arakawa H
- type
- Author
- name
- Kiyokawa N
- type
- Author
- name
- Tomizawa D
- type
- Author
- bibliography ids
- nci-bib-422050631fc938320d1f0d6b
- book metadata
- content sha256
- 1496513fc73f960429b89e4e6e7f1e791386b44ebc5b934e680c45ae959a24f9
- document type
- citation
- dois
- 10.1182/blood-2017-11-814442
- electronic publication date
- display
- 2018 Mar 14
- precision
- day
- year
- 2018
- evidence scope
- bibliographic_metadata_only
- id
- pubmed:29540347
- immutable id
- pubmed:29540347@1496513fc73f960429b89e4e6e7f1e791386b44ebc5b934e680c45ae959a24f9
- journal
- abbreviation
- Blood
- issn electronic
- 1528-0020
- issn print
- 0006-4971
- issue
- 20
- name
- Blood
- nlm unique id
- 7603509
- pages
- 2266-2270
- volume
- 131
- languages
- eng
- notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
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- has retraction in link
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- pubmed marks article retracted
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- relationships
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- pmid
- 29540347
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- NCBI PubMed ESummary
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- 6eef0d8cc09b77e73af656f6390cc734befb84fbc4c229b886e81e5d95bece31
- retrieved at
- 2026-09-09T23:47:30.975610+00:00
- publication date
- display
- 2018 May 17
- precision
- day
- year
- 2018
- publication types
- Letter
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis.
Preserved source evidence · Independent clinical review pending · Not medical advice
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