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Pouria Mashouri

Showing results (11-20 of 14) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Correction: Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classesWillie H Chang, Pouria Mashouri, Alexander X Lozano, et al.
American Journal of Human Genetics|March 5, 2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian DiseaseHernan D Gonorazky, Sergey Naumenko, Arun K Ramani, et al.
Human Mutation|February 19, 2022
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discoveryHannah G Driver, Taila Hartley, E Magda Price, et al.
Plos One|February 16, 2021
Prospective observational study and serosurvey of SARS-CoV-2 infection in asymptomatic healthcare workers at a Canadian tertiary care centerVictor H Ferreira, Andrzej Chruscinski, Vathany Kulasingam, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Correction: Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classesWillie H Chang, Pouria Mashouri, Alexander X Lozano, et al.
American Journal of Human Genetics|March 5, 2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian DiseaseHernan D Gonorazky, Sergey Naumenko, Arun K Ramani, et al.
Human Mutation|February 19, 2022
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discoveryHannah G Driver, Taila Hartley, E Magda Price, et al.
Plos One|February 16, 2021
Prospective observational study and serosurvey of SARS-CoV-2 infection in asymptomatic healthcare workers at a Canadian tertiary care centerVictor H Ferreira, Andrzej Chruscinski, Vathany Kulasingam, et al.
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