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PUBLICATIONS · 22306653

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.

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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
2012 Feb 5
First author
Astuti D

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

    1. name
      Astuti D
      type
      Author
    2. name
      Morris MR
      type
      Author
    3. name
      Cooper WN
      type
      Author
    4. name
      Staals RH
      type
      Author
    5. name
      Wake NC
      type
      Author
    6. name
      Fews GA
      type
      Author
    7. name
      Gill H
      type
      Author
    8. name
      Gentle D
      type
      Author
    9. name
      Shuib S
      type
      Author
    10. name
      Ricketts CJ
      type
      Author
    11. name
      Cole T
      type
      Author
    12. name
      van Essen AJ
      type
      Author
    Complete bibliographic record and source provenance
    authors
    1. name
      Astuti D
      type
      Author
    2. name
      Morris MR
      type
      Author
    3. name
      Cooper WN
      type
      Author
    4. name
      Staals RH
      type
      Author
    5. name
      Wake NC
      type
      Author
    6. name
      Fews GA
      type
      Author
    7. name
      Gill H
      type
      Author
    8. name
      Gentle D
      type
      Author
    9. name
      Shuib S
      type
      Author
    10. name
      Ricketts CJ
      type
      Author
    11. name
      Cole T
      type
      Author
    12. name
      van Essen AJ
      type
      Author
    bibliography ids
    1. nci-bib-b8361b15b2645b5bf7fa1bf4
    book metadata
    content sha256
    5bb6d14dc18f91433eed3a08fbeb67f9f3c0a01e2cfc75dd0bdde91bce88ba78
    document type
    citation
    dois
    1. 10.1038/ng.1071
    electronic publication date
    display
    2012 Feb 5
    precision
    day
    year
    2012
    evidence scope
    bibliographic_metadata_only
    id
    pubmed:22306653
    immutable id
    pubmed:22306653@5bb6d14dc18f91433eed3a08fbeb67f9f3c0a01e2cfc75dd0bdde91bce88ba78
    journal
    abbreviation
    Nat Genet
    issn electronic
    1546-1718
    issn print
    1061-4036
    issue
    3
    name
    Nature genetics
    nlm unique id
    9216904
    pages
    277-84
    volume
    44
    languages
    1. eng
    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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    has retraction in link
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    pubmed marks article retracted
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    pubmed marks retraction notice
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    relationships
      outcomes validated
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      pmid
      22306653
      provenance
      batch id
      b6284687e167e7da9556
      provider
      NCBI PubMed ESummary
      record sha256
      fe4b2ea24a0d0cdfb564ad555ab1dbf4896d84a188d6a197ec886d614592403e
      response sha256
      64d5b7bb63f574c559af2523b779a262267cbc8e8cd02a5b47f4193cc95cabd3
      retrieved at
      2026-09-09T23:46:45.216259+00:00
      publication date
      display
      2012 Feb 5
      precision
      day
      year
      2012
      publication types
      1. Journal Article
      2. 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/22306653/
      title
      Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.

      Preserved source evidence · Independent clinical review pending · Not medical advice