TrianglePUBLICATIONS · 23169491
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
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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
- Eur J Hum Genet
- Publication date
- 2013 Jul
- First author
- Isidor B
Publication notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
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- relationships
Authors and identifiers
- name
- Isidor B
- type
- Author
- name
- Bourdeaut F
- type
- Author
- name
- Lafon D
- type
- Author
- name
- Plessis G
- type
- Author
- name
- Lacaze E
- type
- Author
- name
- Kannengiesser C
- type
- Author
- name
- Rossignol S
- type
- Author
- name
- Pichon O
- type
- Author
- name
- Briand A
- type
- Author
- name
- Martin-Coignard D
- type
- Author
- name
- Piccione M
- type
- Author
- name
- David A
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Isidor B
- type
- Author
- name
- Bourdeaut F
- type
- Author
- name
- Lafon D
- type
- Author
- name
- Plessis G
- type
- Author
- name
- Lacaze E
- type
- Author
- name
- Kannengiesser C
- type
- Author
- name
- Rossignol S
- type
- Author
- name
- Pichon O
- type
- Author
- name
- Briand A
- type
- Author
- name
- Martin-Coignard D
- type
- Author
- name
- Piccione M
- type
- Author
- name
- David A
- type
- Author
- bibliography ids
- nci-bib-34b43f52922b463556aa3f57
- book metadata
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- 6e78bd7d06c9bebf247d5590f24e6b50d66e597d0632e1aebc5251b0f3cee585
- document type
- citation
- dois
- 10.1038/ejhg.2012.252
- electronic publication date
- display
- 2012 Nov 21
- precision
- day
- year
- 2012
- evidence scope
- bibliographic_metadata_only
- id
- pubmed:23169491
- immutable id
- pubmed:23169491@6e78bd7d06c9bebf247d5590f24e6b50d66e597d0632e1aebc5251b0f3cee585
- journal
- abbreviation
- Eur J Hum Genet
- issn electronic
- 1476-5438
- issn print
- 1018-4813
- issue
- 7
- name
- European journal of human genetics : EJHG
- nlm unique id
- 9302235
- pages
- 784-7
- volume
- 21
- languages
- eng
- notices
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- has correction metadata
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- retrieved at
- 2026-09-09T23:46:52.860383+00:00
- publication date
- display
- 2013 Jul
- precision
- month
- year
- 2013
- publication types
- Journal Article
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
Preserved source evidence · Independent clinical review pending · Not medical advice