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Ugeskrift for Laeger
|
June 11, 2025
[Renal tumours]
Marwah Jasim Hussein Hussein, Malene Lundsgaard, Mia Gebauer Madsen, et al.
BMJ Case Reports
|
July 29, 2025
Mosaicism for a variant in <i>PTCH1</i> causing nevoid basal cell carcinoma syndrome
Inger Norlyk Sheyanth, Mette Sommerlund, Hanne Vinter, et al.
Ugeskrift for Laeger
|
November 28, 2025
[Metachronous colon cancer after successful treatment of mismatch repair-deficient metastatic colorectal cancer]
Line Hansen, Michael Bødker Lauritzen, Christian Thomsen, et al.
Molecular Syndromology
|
February 25, 2017
De novo <i>KAT6B</i> Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome
Malene Lundsgaard, Vang Q Le, Anja Ernst, et al.
Clinical Genetics
|
April 12, 2024
Expanding the understanding of telomere biology disorder with reports from two families harboring variants in ZCCHC8 and TERC
Nikolaj Juul Nitschke, Anne Marie Jelsig, Charlotte Lautrup, et al.
Journal of Medical Genetics
|
April 5, 2023
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort
Ulrik Kristoffer Stoltze, Mathis Hildonen, Thomas Van Overeem Hansen, et al.
Human Genetics
|
July 29, 2022
Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer
Malene Djursby, Thomas van Overeem Hansen, Karin A W Wadt, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Ugeskrift for Laeger
|
June 11, 2025
[Renal tumours]
Marwah Jasim Hussein Hussein, Malene Lundsgaard, Mia Gebauer Madsen, et al.
BMJ Case Reports
|
July 29, 2025
Mosaicism for a variant in <i>PTCH1</i> causing nevoid basal cell carcinoma syndrome
Inger Norlyk Sheyanth, Mette Sommerlund, Hanne Vinter, et al.
Ugeskrift for Laeger
|
November 28, 2025
[Metachronous colon cancer after successful treatment of mismatch repair-deficient metastatic colorectal cancer]
Line Hansen, Michael Bødker Lauritzen, Christian Thomsen, et al.
Molecular Syndromology
|
February 25, 2017
De novo <i>KAT6B</i> Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome
Malene Lundsgaard, Vang Q Le, Anja Ernst, et al.
Clinical Genetics
|
April 12, 2024
Expanding the understanding of telomere biology disorder with reports from two families harboring variants in ZCCHC8 and TERC
Nikolaj Juul Nitschke, Anne Marie Jelsig, Charlotte Lautrup, et al.
Journal of Medical Genetics
|
April 5, 2023
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort
Ulrik Kristoffer Stoltze, Mathis Hildonen, Thomas Van Overeem Hansen, et al.
Human Genetics
|
July 29, 2022
Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer
Malene Djursby, Thomas van Overeem Hansen, Karin A W Wadt, et al.
Page
of 1