TrianglePUBLICATIONS · 33896058
Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney.
Open original source → · Download preserved record
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
- 2021 Aug
- First author
- Haruta M
Publication notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
- false
- has retraction in link
- false
- pubmed marks article retracted
- false
- pubmed marks retraction notice
- false
- relationships
Authors and identifiers
- name
- Haruta M
- type
- Author
- name
- Arai Y
- type
- Author
- name
- Okita H
- type
- Author
- name
- Tanaka Y
- type
- Author
- name
- Takimoto T
- type
- Author
- name
- Kamijo T
- type
- Author
- name
- Oue T
- type
- Author
- name
- Souzaki R
- type
- Author
- name
- Taguchi T
- type
- Author
- name
- Kuwahara Y
- type
- Author
- name
- Chin M
- type
- Author
- name
- Nakadate H
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Haruta M
- type
- Author
- name
- Arai Y
- type
- Author
- name
- Okita H
- type
- Author
- name
- Tanaka Y
- type
- Author
- name
- Takimoto T
- type
- Author
- name
- Kamijo T
- type
- Author
- name
- Oue T
- type
- Author
- name
- Souzaki R
- type
- Author
- name
- Taguchi T
- type
- Author
- name
- Kuwahara Y
- type
- Author
- name
- Chin M
- type
- Author
- name
- Nakadate H
- type
- Author
- bibliography ids
- nci-bib-93ee07e7ae223f155733eb22
- book metadata
- content sha256
- 6214a11e95353537fbc2966bbb0f87634d9d082563cb9c3e1af0537954fff1a3
- document type
- citation
- dois
- 10.1002/gcc.22952
- electronic publication date
- display
- 2021 May 4
- precision
- day
- year
- 2021
- evidence scope
- bibliographic_metadata_only
- id
- pubmed:33896058
- immutable id
- pubmed:33896058@6214a11e95353537fbc2966bbb0f87634d9d082563cb9c3e1af0537954fff1a3
- journal
- abbreviation
- Genes Chromosomes Cancer
- issn electronic
- 1098-2264
- issn print
- 1045-2257
- issue
- 8
- name
- Genes, chromosomes & cancer
- nlm unique id
- 9007329
- pages
- 546-558
- volume
- 60
- languages
- eng
- notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
- false
- has retraction in link
- false
- pubmed marks article retracted
- false
- pubmed marks retraction notice
- false
- relationships
- outcomes validated
- false
- pmid
- 33896058
- provenance
- batch id
- 79f1021053e858d13ff3
- provider
- NCBI PubMed ESummary
- record sha256
- a968c1de84fb9c9a2122c4ed2f7434024129276f4c93c1b51178560956f06c8e
- response sha256
- 671d3d2962f73c698a1cb338d73222e2cc6cfdf61569f91b42612d5b59822e05
- retrieved at
- 2026-09-09T23:47:59.098265+00:00
- publication date
- display
- 2021 Aug
- precision
- month
- year
- 2021
- publication types
- Journal Article
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney.
Preserved source evidence · Independent clinical review pending · Not medical advice