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Rigshospitalet - a part of Copenhagen University Hospital
Published

Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)-an update

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  1. The genetic structure of Norway

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  2. Atrial fibrillation-a complex polygenetic disease

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  3. Direct to consumer genetic testing in Denmark-public knowledge, use, and attitudes

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  4. Forming and ending marital or cohabiting relationships in a Danish population-based cohort of individuals with neurofibromatosis 1

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  5. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

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  1. Genetic disease is a common cause of bilateral childhood cataract in Denmark

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  2. Genotype-phenotype associations in Danish patients with ocular and oculocutaneous albinism

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement

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Original languageEnglish
JournalEuropean journal of human genetics : EJHG
Volume29
Issue number10
Pages (from-to)1577-1583
Number of pages7
ISSN1018-4813
DOIs
Publication statusPublished - Oct 2021

ID: 62034661