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Ugeskrift for Laeger
|
November 15, 2014
[Medical genetics and the genome]
Anne-Marie Gerdes, Ida Vogel
Human Genome Variation
|
October 25, 2019
A new family with a homozygous nonsense variant in <i>NTHL1</i> further delineated the clinical phenotype of <i>NTHL1</i>-associated polyposis
Mays Altaraihi, Anne-Marie Gerdes, Karin Wadt
Ugeskrift for Laeger
|
October 14, 2006
[Press, ethics and genetic screening]
Anne-Marie Gerdes, Karen Brøndum-Nielsen, Bent Ejlertsen
Ugeskrift for Laeger
|
March 18, 2014
[Cowden syndrome can be a challenging diagnosis]
Anne-Bine Skytte, Anne-Marie Gerdes, Anette Bygum
Ugeskrift 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 generations
Sigurd Broesby-Olsen, Anette Bygum, Anne-Marie Gerdes, et al.
Familial Cancer
|
June 22, 2015
High accuracy of family history of melanoma in Danish melanoma cases
Karin A W Wadt, Krzysztof T Drzewiecki, Anne-Marie Gerdes
Gynecologic Oncology
|
March 18, 2014
The results of gynecologic surveillance in families with hereditary nonpolyposis colorectal cancer
Zohreh Ketabi, Anne-Marie Gerdes, Berit Mosgaard, et al.
Breast Cancer : Basic and Clinical Research
|
November 5, 2014
Hereditary breast cancer: clinical, pathological and molecular characteristics
Martin 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 13
Mads Thomassen, Torben A Kruse, Peter K A Jensen, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 159) with videos related to
Sort By:
Page
of 16
Ugeskrift for Laeger
|
November 15, 2014
[Medical genetics and the genome]
Anne-Marie Gerdes, Ida Vogel
Human Genome Variation
|
October 25, 2019
A new family with a homozygous nonsense variant in <i>NTHL1</i> further delineated the clinical phenotype of <i>NTHL1</i>-associated polyposis
Mays Altaraihi, Anne-Marie Gerdes, Karin Wadt
Ugeskrift for Laeger
|
October 14, 2006
[Press, ethics and genetic screening]
Anne-Marie Gerdes, Karen Brøndum-Nielsen, Bent Ejlertsen
Ugeskrift for Laeger
|
March 18, 2014
[Cowden syndrome can be a challenging diagnosis]
Anne-Bine Skytte, Anne-Marie Gerdes, Anette Bygum
Ugeskrift 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 generations
Sigurd Broesby-Olsen, Anette Bygum, Anne-Marie Gerdes, et al.
Familial Cancer
|
June 22, 2015
High accuracy of family history of melanoma in Danish melanoma cases
Karin A W Wadt, Krzysztof T Drzewiecki, Anne-Marie Gerdes
Gynecologic Oncology
|
March 18, 2014
The results of gynecologic surveillance in families with hereditary nonpolyposis colorectal cancer
Zohreh Ketabi, Anne-Marie Gerdes, Berit Mosgaard, et al.
Breast Cancer : Basic and Clinical Research
|
November 5, 2014
Hereditary breast cancer: clinical, pathological and molecular characteristics
Martin 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 13
Mads Thomassen, Torben A Kruse, Peter K A Jensen, et al.
Page
of 16