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PUBLICATIONS · 16646086

High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.

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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
Genes Chromosomes Cancer
Publication date
2006 Aug
First author
von Bergh AR

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
      von Bergh AR
      type
      Author
    2. name
      van Drunen E
      type
      Author
    3. name
      van Wering ER
      type
      Author
    4. name
      van Zutven LJ
      type
      Author
    5. name
      Hainmann I
      type
      Author
    6. name
      Lönnerholm G
      type
      Author
    7. name
      Meijerink JP
      type
      Author
    8. name
      Pieters R
      type
      Author
    9. name
      Beverloo HB
      type
      Author
    Complete bibliographic record and source provenance
    authors
    1. name
      von Bergh AR
      type
      Author
    2. name
      van Drunen E
      type
      Author
    3. name
      van Wering ER
      type
      Author
    4. name
      van Zutven LJ
      type
      Author
    5. name
      Hainmann I
      type
      Author
    6. name
      Lönnerholm G
      type
      Author
    7. name
      Meijerink JP
      type
      Author
    8. name
      Pieters R
      type
      Author
    9. name
      Beverloo HB
      type
      Author
    bibliography ids
    1. nci-bib-4b10c51aacb5c0ffcaae7cf9
    book metadata
    content sha256
    d33b1dcff2cb2905c6aad18718b255253d1a56e937e263eaa66e41cc64978b49
    document type
    citation
    dois
    1. 10.1002/gcc.20335
    electronic publication date
    display
    Source null
    precision
    missing
    year
    Source null
    evidence scope
    bibliographic_metadata_only
    id
    pubmed:16646086
    immutable id
    pubmed:16646086@d33b1dcff2cb2905c6aad18718b255253d1a56e937e263eaa66e41cc64978b49
    journal
    abbreviation
    Genes Chromosomes Cancer
    issn electronic
    Source null
    issn print
    1045-2257
    issue
    8
    name
    Genes, chromosomes & cancer
    nlm unique id
    9007329
    pages
    731-9
    volume
    45
    languages
    1. 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
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    pubmed marks retraction notice
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    relationships
      outcomes validated
      false
      pmid
      16646086
      provenance
      batch id
      19fb2de9a00882c94e86
      provider
      NCBI PubMed ESummary
      record sha256
      f3683cd9c0d4fd8b7be94370dc358d8c28301ba70b0a20bb57e7aeca78a5d14f
      response sha256
      4c446464d8fd06bff771a2bb5f3529ef4abe372e3c19f6fb7223068d839a263d
      retrieved at
      2026-09-09T23:46:06.810486+00:00
      publication date
      display
      2006 Aug
      precision
      month
      year
      2006
      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/16646086/
      title
      High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.

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