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Pål Møller

Showing results (1-10 of 95) with videos related to

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Hereditary Cancer in Clinical Practice|November 21, 2022
The Prospective Lynch Syndrome Database: background, design, main results and complete MySQL codePål Møller
Hereditary Cancer in Clinical Practice|March 20, 2020
The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health carePål Møller
Hereditary Cancer in Clinical Practice|March 18, 2010
Towards evidence-based management of inherited breast and breast-ovarian cancerPål Møller
Medicine, Health Care, and Philosophy|September 24, 2017
Our genes, our selves: hereditary breast cancer and biological citizenship in NorwayPål Møller, Eivind Hovig
Hereditary Cancer in Clinical Practice|May 11, 2018
Retraction Note to: The <i>BRCA2</i> variant c.68-7 T > A is associated with breast cancerPål Møller, Eivind Hovig
Hereditary Cancer in Clinical Practice|November 22, 2017
The <i>BRCA2</i> variant c.68-7 T>A is associated with breast cancerPål Møller, Eivind Hovig
Human Mutation|March 10, 2011
CGEN--a Clinical GENetics software applicationPål Møller, Neal Clark
Journal of Clinical Medicine|February 15, 2022
Inherited Cancer Genetic Epidemiology to Improve Precision MedicinePål Møller, Dafydd Gareth Evans
Human Mutation|February 11, 2011
A SImplified method for Segregation Analysis (SISA) to determine penetrance and expression of a genetic variant in a familyPål Møller, Neal Clark, Lovise Mæhle
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 22, 2005
[Hereditary breast cancer]Pål Møller, Lovise Maehle, Jaran Apold
Pageof 10

Showing results (1-10 of 95) with videos related to

Sort By:
Pageof 10
Hereditary Cancer in Clinical Practice|November 21, 2022
The Prospective Lynch Syndrome Database: background, design, main results and complete MySQL codePål Møller
Hereditary Cancer in Clinical Practice|March 20, 2020
The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health carePål Møller
Hereditary Cancer in Clinical Practice|March 18, 2010
Towards evidence-based management of inherited breast and breast-ovarian cancerPål Møller
Medicine, Health Care, and Philosophy|September 24, 2017
Our genes, our selves: hereditary breast cancer and biological citizenship in NorwayPål Møller, Eivind Hovig
Hereditary Cancer in Clinical Practice|May 11, 2018
Retraction Note to: The <i>BRCA2</i> variant c.68-7 T > A is associated with breast cancerPål Møller, Eivind Hovig
Hereditary Cancer in Clinical Practice|November 22, 2017
The <i>BRCA2</i> variant c.68-7 T>A is associated with breast cancerPål Møller, Eivind Hovig
Human Mutation|March 10, 2011
CGEN--a Clinical GENetics software applicationPål Møller, Neal Clark
Journal of Clinical Medicine|February 15, 2022
Inherited Cancer Genetic Epidemiology to Improve Precision MedicinePål Møller, Dafydd Gareth Evans
Human Mutation|February 11, 2011
A SImplified method for Segregation Analysis (SISA) to determine penetrance and expression of a genetic variant in a familyPål Møller, Neal Clark, Lovise Mæhle
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 22, 2005
[Hereditary breast cancer]Pål Møller, Lovise Maehle, Jaran Apold
Pageof 10