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  • Verberne, EA (author)

JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome

  • Article/chapterEnglish2021

Publisher, publication year, extent ...

  • Elsevier BV,2021

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:144987546
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:144987546URI
  • https://doi.org/10.1038/s41436-020-00992-zDOI

Supplementary language notes

  • Language:English

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Classification

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

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

  • Goh, SX (author)
  • England, J (author)
  • van Ginkel, M (author)
  • Rafael-Croes, L (author)
  • Maas, S (author)
  • Polstra, A (author)
  • Zarate, YA (author)
  • Bosanko, KA (author)
  • Pechter, KB (author)
  • Bedoukian, E (author)
  • Izumi, K (author)
  • Chaudhry, A (author)
  • Robin, NH (author)
  • Boothe, M (author)
  • Lippa, NC (author)
  • Aggarwal, V (author)
  • De Vivo, DC (author)
  • Lehman, A (author)
  • Stockler, S (author)
  • Bruel, AL (author)
  • Isidor, B (author)
  • Lemons, J (author)
  • Rodriguez-Buritica, DF (author)
  • Richmond, CM (author)
  • Stark, Z (author)
  • Agrawal, PB (author)
  • Kooy, RF (author)
  • Meuwissen, MEC (author)
  • Koolen, DA (author)
  • Pfundt, R (author)
  • Lieden, AKarolinska Institutet (author)
  • Anderlid, BMKarolinska Institutet (author)
  • Glatz, D (author)
  • Mannens, MMAM (author)
  • Bakshi, M (author)
  • Mallette, FA (author)
  • van Haelst, MM (author)
  • Campeau, PM (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:Genetics in medicine : official journal of the American College of Medical Genetics: Elsevier BV23:2, s. 374-3831530-0366
  • In:Genetics in Medicine: Elsevier BV23:2, s. 374-3831098-3600

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