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Search: onr:"swepub:oai:prod.swepub.kib.ki.se:112272808" > A new chromosome 17...

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  • Koolen, DA (author)

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

  • Article/chapterEnglish2006

Publisher, publication year, extent ...

  • 2006-08-13
  • Springer Science and Business Media LLC,2006

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:112272808
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:112272808URI
  • https://doi.org/10.1038/ng1853DOI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Added entries (persons, corporate bodies, meetings, titles ...)

  • Vissers, LELM (author)
  • Pfundt, R (author)
  • de Leeuw, N (author)
  • Knight, SJL (author)
  • Regan, R (author)
  • Kooy, RF (author)
  • Reyniers, E (author)
  • Romano, C (author)
  • Fichera, M (author)
  • Schinzel, A (author)
  • Baumer, A (author)
  • Anderlid, BMKarolinska Institutet (author)
  • Schoumans, JKarolinska Institutet (author)
  • Knoers, NV (author)
  • van Kessel, AG (author)
  • Sistermans, EA (author)
  • Veltman, JA (author)
  • Brunner, HG (author)
  • de Vries, BBA (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:Nature genetics: Springer Science and Business Media LLC38:9, s. 999-10011061-40361546-1718

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