TrianglePUBLICATIONS · 9398852
Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
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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
- Nat Genet
- Publication date
- 1997 Dec
- First author
- Barbaux S
Publication notices
- absence is not clearance
- true
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- false
- has expression of concern metadata
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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
- Barbaux S
- type
- Author
- name
- Niaudet P
- type
- Author
- name
- Gubler MC
- type
- Author
- name
- Grünfeld JP
- type
- Author
- name
- Jaubert F
- type
- Author
- name
- Kuttenn F
- type
- Author
- name
- Fékété CN
- type
- Author
- name
- Souleyreau-Therville N
- type
- Author
- name
- Thibaud E
- type
- Author
- name
- Fellous M
- type
- Author
- name
- McElreavey K
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Barbaux S
- type
- Author
- name
- Niaudet P
- type
- Author
- name
- Gubler MC
- type
- Author
- name
- Grünfeld JP
- type
- Author
- name
- Jaubert F
- type
- Author
- name
- Kuttenn F
- type
- Author
- name
- Fékété CN
- type
- Author
- name
- Souleyreau-Therville N
- type
- Author
- name
- Thibaud E
- type
- Author
- name
- Fellous M
- type
- Author
- name
- McElreavey K
- type
- Author
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- document type
- citation
- dois
- 10.1038/ng1297-467
- electronic publication date
- display
- Source null
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- missing
- year
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- bibliographic_metadata_only
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- pubmed:9398852
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- journal
- abbreviation
- Nat Genet
- issn electronic
- Source null
- issn print
- 1061-4036
- issue
- 4
- name
- Nature genetics
- nlm unique id
- 9216904
- pages
- 467-70
- volume
- 17
- languages
- eng
- notices
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- retrieved at
- 2026-09-09T23:45:29.081942+00:00
- publication date
- display
- 1997 Dec
- precision
- month
- year
- 1997
- publication types
- Case Reports
- Journal Article
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- source url
- https://pubmed.ncbi.nlm.nih.gov/9398852/
- title
- Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
Preserved source evidence · Independent clinical review pending · Not medical advice