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Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]Anne Marie Jelsig, Pernille Mathiesen Tørring, Niels Qvist, et al.
European Journal of Medical Genetics|November 21, 2016
Novel ELN mutation in a family with supravalvular aortic stenosis and intracranial aneurysmAnne Marie Jelsig, Zsolt Urban, Vishwanathan Hucthagowder, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]Anne Marie Jelsig, Pernille Mathiesen Tørring, Niels Qvist, et al.
Scandinavian Journal of Gastroenterology|October 6, 2022
Preimplantation genetic testing in two Danish couples affected by Peutz-Jeghers syndromeAnna Byrjalsen, Laura Roos, Tue Diemer, et al.
Hereditary Cancer in Clinical Practice|May 15, 2023
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeresAnna Byrjalsen, Anna Engell Brainin, Thomas Kromann Lund, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation]Anne Marie Jelsig, Pernille Mathiesen Tørring, Friedrik Wikman, et al.
United European Gastroenterology Journal|July 27, 2023
Cancer risk and mortality in patients with solitary juvenile polyps-A nationwide cohort study with matched controlsAnne Marie Jelsig, Laus Wullum, Tine Plato Kuhlmann, et al.
Ugeskrift for Laeger|September 1, 2015
[Noonan syndrome can be diagnosed clinically and through molecular genetic analyses]Marie Krab Henningsen, Anne Marie Jelsig, Helle Andersen, et al.
Orphanet Journal of Rare Diseases|July 16, 2014
Hamartomatous polyposis syndromes: a reviewAnne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
Journal of Medical Genetics|August 29, 2022
Hereditary haemorrhagic telangiectasia in Danish patients with pathogenic variants in SMAD4: a nationwide studyAnne Marie Jelsig, Anette Kjeldsen, Lise Lotte Christensen, et al.
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