PUBLICATIONS · 23636228
Long-term follow-up of ETV6-RUNX1 ALL reveals that NCI risk, rather than secondary genetic abnormalities, is the key risk factor.
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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
- Leukemia
- Publication date
- 2013 Nov
- First author
- Enshaei A
Publication notices
- absence is not clearance
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- has correction metadata
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- has expression of concern metadata
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- relationships
Authors and identifiers
- name
- Enshaei A
- type
- Author
- name
- Schwab CJ
- type
- Author
- name
- Konn ZJ
- type
- Author
- name
- Mitchell CD
- type
- Author
- name
- Kinsey SE
- type
- Author
- name
- Wade R
- type
- Author
- name
- Vora A
- type
- Author
- name
- Harrison CJ
- type
- Author
- name
- Moorman AV
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Enshaei A
- type
- Author
- name
- Schwab CJ
- type
- Author
- name
- Konn ZJ
- type
- Author
- name
- Mitchell CD
- type
- Author
- name
- Kinsey SE
- type
- Author
- name
- Wade R
- type
- Author
- name
- Vora A
- type
- Author
- name
- Harrison CJ
- type
- Author
- name
- Moorman AV
- type
- Author
- bibliography ids
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- 3a11e8587db09019fd5537f7089e78bdc22aa2cba22a1dded117d5ff54503efd
- document type
- citation
- dois
- 10.1038/leu.2013.136
- electronic publication date
- display
- 2013 May 2
- precision
- day
- year
- 2013
- evidence scope
- bibliographic_metadata_only
- id
- pubmed:23636228
- immutable id
- pubmed:23636228@3a11e8587db09019fd5537f7089e78bdc22aa2cba22a1dded117d5ff54503efd
- journal
- abbreviation
- Leukemia
- issn electronic
- 1476-5551
- issn print
- 0887-6924
- issue
- 11
- name
- Leukemia
- nlm unique id
- 8704895
- pages
- 2256-9
- volume
- 27
- languages
- eng
- notices
- absence is not clearance
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- has expression of concern metadata
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- 23636228
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- retrieved at
- 2026-09-09T23:46:55.094762+00:00
- publication date
- display
- 2013 Nov
- precision
- month
- year
- 2013
- publication types
- Letter
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- Long-term follow-up of ETV6-RUNX1 ALL reveals that NCI risk, rather than secondary genetic abnormalities, is the key risk factor.
Preserved source evidence · Independent clinical review pending · Not medical advice
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