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Region Hovedstaden - en del af Københavns Universitetshospital
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Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci

Publikation: AndetAndet bidragForskning

DOI

  1. Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A)

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohorts

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  • Thomas Eggermann
  • Guiomar Perez de Nanclares
  • Eamonn R Maher
  • I Karen Temple
  • Zeynep Tümer
  • David Monk
  • Deborah J G Mackay
  • Karen Grønskov
  • Andrea Riccio
  • Agnès Linglart
  • Irène Netchine
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[This corrects the article DOI: 10.1186/s13148-015-0143-8.].

OriginalsprogEngelsk
Publikationsdato2016
Vol/bind8
DOI
StatusUdgivet - 2016
NavnClinical Epigenetics
ISSN1868-7075
No renderer: associatesEventPortal,dk.atira.pure.api.shared.model.researchoutput.OtherContribution

ID: 50109698