TrianglePUBLICATIONS · 12070009
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease.
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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
- 2002 Jul 1
- First author
- Schnittger S
Publication notices
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Authors and identifiers
- name
- Schnittger S
- type
- Author
- name
- Schoch C
- type
- Author
- name
- Dugas M
- type
- Author
- name
- Kern W
- type
- Author
- name
- Staib P
- type
- Author
- name
- Wuchter C
- type
- Author
- name
- Löffler H
- type
- Author
- name
- Sauerland CM
- type
- Author
- name
- Serve H
- type
- Author
- name
- Büchner T
- type
- Author
- name
- Haferlach T
- type
- Author
- name
- Hiddemann W
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Schnittger S
- type
- Author
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- Schoch C
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- Dugas M
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- Kern W
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- Staib P
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- Wuchter C
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- Löffler H
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- Sauerland CM
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- Serve H
- type
- Author
- name
- Büchner T
- type
- Author
- name
- Haferlach T
- type
- Author
- name
- Hiddemann W
- type
- Author
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- document type
- citation
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- 10.1182/blood.v100.1.59
- electronic publication date
- display
- Source null
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- missing
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- bibliographic_metadata_only
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- pubmed:12070009
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- pubmed:12070009@5329aaba7adc0abbae3cb9c61ed0964d636fff525dd023f39ea164a9b7ccd919
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- Blood
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- 0006-4971
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- 1
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- Blood
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- 7603509
- pages
- 59-66
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- 100
- languages
- eng
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- retrieved at
- 2026-09-09T23:45:46.208577+00:00
- publication date
- display
- 2002 Jul 1
- precision
- day
- year
- 2002
- publication types
- Journal Article
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease.
Preserved source evidence · Independent clinical review pending · Not medical advice