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  1. Rigshospitalet
  2. Forskere
  3. Lisbeth Tranebjærg
Rigshospitalet - en del af Københavns Universitetshospital

Lisbeth Tranebjærg

MD PhD

Bygning: ,

Danmark

Seneste publikationer Vis alle (60) »

  1. Udgivet

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

    Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

  2. E-pub ahead of print

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

    Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

  3. E-pub ahead of print

    Functional Assessment of Variants Associated with Wolfram Syndrome

    Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Mest brugte tidsskrifter Vis alle »

  1. European Journal of Human Genetics

    ISSN'er: 1018-4813

    Yderligere søgbare ISSNs (Elektroniske): 1476-5438

    Nature Publishing Group, Storbritannien

    Tidsskrift

  2. Human Mutation

    ISSN'er: 1059-7794

    Yderligere søgbare ISSNs (Elektroniske): 1098-1004

    John/Wiley & Sons, Inc. John/Wiley & Sons Ltd, USA

    Tidsskrift

  3. Movement Disorders

    ISSN'er: 0885-3185

    Yderligere søgbare ISSNs (Elektroniske): 1531-8257

    John/Wiley & Sons, Inc. John/Wiley & Sons Ltd, USA

    Tidsskrift

  4. Human Molecular Genetics

    ISSN'er: 0964-6906

    Yderligere søgbare ISSNs (Elektroniske): 1460-2083

    Oxford University Press, Storbritannien

    Tidsskrift

  5. Medical Genetics Information Resource

    Copyright, University of Washington, Seattle. 1997-2008

    Tidsskrift

Mest brugte forlag Vis alle »

  1. Springer Publishing Company

    USA

    Forlag

  2. Nova Science Publishers, Incorporated

    USA

    Forlag

Vis graf over relationer

Expertise

Clinical genetics, especially hereditary hearing impairment and dual sensory impairment (deaf-blindness.

Primære forskningsområder

Genetics of deafness and hearing impairment, dual sensory impairment (deaf-blindness); Ethics of clinical genetics and advanced sequencing methods (next generation sequencing)

Aktuel forskning

As above

Mulige interessekonflikter

none

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