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Rigshospitalet - a part of Copenhagen University Hospital
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Genetisk screening af kommende forældre

Research output: Contribution to journalReviewpeer-review

  1. MR-vejledt laserablation til behandling af hjernetumorer og epilepsi

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  2. Børn med iskæmisk apopleksi

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  3. Dual-energy CT

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  4. Paradox embolism in a patient with pulmonary embolism and unknown patent foramen ovale

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  5. Genetisk screening af adopterede raske individer

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  1. Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families

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  3. Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

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  4. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

    Research output: Contribution to journalJournal articleResearchpeer-review

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

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Risk of genetic diseases with autosomal recessive or X-linked inheritance can be unknown to prospective parents until an affected child is born. New technology has enabled carrier screening for hundreds of genetic diseases (expanded carrier screening, ECS). I Denmark, each year estimated 100-180 children are born affected with a serious condition which could have been detected with ECS of the parents. This review describes the considerations and perspectives of a systematic genetic screening programme for prospective parents in the Danish healthcare system.

Translated title of the contributionGenetic screening of prospective parents
Original languageDanish
JournalUgeskrift for Laeger
Volume183
Issue number13
ISSN0041-5782
Publication statusPublished - 29 Mar 2021

ID: 65147392