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American Journal of Human Genetics|November 9, 2021
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilizationCarrie L Blout Zawatsky, Nidhi Shah, Kalotina Machini, et al.
International Journal of Cancer|December 21, 2010
Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancerAung Ko Win, Sean P Cleary, James G Dowty, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 6, 2005
High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genesMichael O Woods, Angela J Hyde, Fiona K Curtis, et al.
Virology|November 24, 2012
Longitudinal study of seroprevalence and serostability of 34 human papillomavirus types in European organ transplant recipientsAnnika Antonsson, Tim Waterboer, Jan N Bouwes Bavinck, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2018
Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case reportJaclyn B Murry, Kalotina Machini, Ozge Ceyhan-Birsoy, et al.
Annals of Internal Medicine|June 28, 2017
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized TrialJason L Vassy, Kurt D Christensen, Erica F Schonman, et al.
Biorxiv : the Preprint Server for Biology|June 9, 2020
A Cryptic Site of Vulnerability on the Receptor Binding Domain of the SARS-CoV-2 Spike GlycoproteinM Gordon Joyce, Rajeshwer S Sankhala, Wei-Hung Chen, et al.
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