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European Journal of Human Genetics : EJHG|October 14, 2024
Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centresCristina Fortuno, Elisa J Cops, Aimee L Davidson, et al.
Breast Cancer Research and Treatment|April 17, 2016
Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypesKristen S Purrington, Daniel W Visscher, Chen Wang, et al.
American Journal of Human Genetics|February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationGuy Froyen, Mark Corbett, Joke Vandewalle, et al.
Neurology|February 24, 2019
Genome-wide association meta-analysis of functional outcome after ischemic strokeMartin Söderholm, Annie Pedersen, Erik Lorentzen, et al.
American Journal of Human Genetics|June 9, 2004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35Mary L Marazita, Jeffrey C Murray, Andrew C Lidral, et al.
Hereditary Cancer in Clinical Practice|October 11, 2023
Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statementPal Møller, Toni T Seppälä, Aysel Ahadova, et al.
Hereditary Cancer in Clinical Practice|March 13, 2019
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportToni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 31, 2018
Cancer Risks for PMS2-Associated Lynch SyndromeSanne W Ten Broeke, Heleen M van der Klift, Carli M J Tops, et al.
Plos One|February 9, 2013
Genome-wide association study of retinopathy in individuals without diabetesRichard A Jensen, Xueling Sim, Xiaohui Li, et al.
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