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Human Genome Variation|October 25, 2019
A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposisMays Altaraihi, Anne-Marie Gerdes, Karin WadtUgeskrift for Laeger|March 18, 2014
[Cowden syndrome can be a challenging diagnosis]Anne-Bine Skytte, Anne-Marie Gerdes, Anette BygumUgeskrift for Laeger|January 29, 2009
[LEOPARD syndrome]Lars Kjaersgård Hansen, Kirsten Risby, Anette Bygum, et al.Acta Dermato-Venereologica|January 8, 2008
Multiple self-healing squamous epithelioma of Ferguson-Smith: observations in a Danish family covering four generationsSigurd Broesby-Olsen, Anette Bygum, Anne-Marie Gerdes, et al.Familial Cancer|June 22, 2015
High accuracy of family history of melanoma in Danish melanoma casesKarin A W Wadt, Krzysztof T Drzewiecki, Anne-Marie GerdesGynecologic Oncology|March 18, 2014
The results of gynecologic surveillance in families with hereditary nonpolyposis colorectal cancerZohreh Ketabi, Anne-Marie Gerdes, Berit Mosgaard, et al.Breast Cancer : Basic and Clinical Research|November 5, 2014
Hereditary breast cancer: clinical, pathological and molecular characteristicsMartin J Larsen, Mads Thomassen, Anne-Marie Gerdes, et al.Genetic Testing|June 24, 2006
A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13Mads Thomassen, Torben A Kruse, Peter K A Jensen, et al.Ugeskrift for Laeger|May 30, 2012
[A new genetic diagnosis of familiar gastrointestinal stromal tumour]Karin Wadt, Mette Klarskov Andersen, Thomas V O Hansen, et al.Pageof 30