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Rigshospitalet - en del af Københavns Universitetshospital
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Corrigendum: Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

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  1. Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndrome

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Functional Assessment of Variants Associated with Wolfram Syndrome

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  4. Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

    Publikation: Bidrag til tidsskriftLetterForskningpeer review

  • Wybo Dondorp
  • Guido de Wert
  • Yvonne Bombard
  • Diana W Bianchi
  • Carsten Bergmann
  • Pascal Borry
  • Lyn S Chitty
  • Florence Fellmann
  • Francesca Forzano
  • Alison Hall
  • Lidewij Henneman
  • Heidi C Howard
  • Anneke Lucassen
  • Kelly Ormond
  • Borut Peterlin
  • Dragica Radojkovic
  • Wolf Rogowski
  • Maria Soller
  • Aad Tibben
  • Lisbeth Tranebjærg
  • Carla G van El
  • Martina C Cornel
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OriginalsprogEngelsk
Publikationsdatonov. 2015
Vol/bind23
DOI
StatusUdgivet - nov. 2015
NavnEuropean journal of human genetics : EJHG
ISSN1018-4813
No renderer: associatesEventPortal,dk.atira.pure.api.shared.model.researchoutput.OtherContribution

ID: 46184701