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Anastasia Fedick

Showing results (1-10 of 9) with videos related to

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Genomics|January 28, 2012
Development of TaqMan allelic discrimination based genotyping of large DNA deletionsAnastasia Fedick, Jing Su, Nathan R Treff
BMC Research Notes|October 23, 2012
High-throughput real-time PCR-based genotyping without DNA purificationAnastasia Fedick, Jing Su, Chaim Jalas, et al.
Fertility and Sterility|January 15, 2013
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic diseaseNathan R Treff, Anastasia Fedick, Xin Tao, et al.
Plos One|April 5, 2013
High-throughput carrier screening using TaqMan allelic discriminationAnastasia Fedick, Jing Su, Chaim Jalas, et al.
The Journal of Molecular Diagnostics : JMD|January 17, 2016
Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk AssessmentJinglan Zhang, Anastasia Fedick, Stephanie Wasserman, et al.
Journal of Medical Genetics|September 14, 2013
Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposisSimon Edvardson, Angel Ashikov, Chaim Jalas, et al.
Journal of Medical Genetics|January 22, 2016
Deficiency of the alkaline ceramidase ACER3 manifests in early childhood by progressive leukodystrophySimon Edvardson, Jae Kyo Yi, Chaim Jalas, et al.
Molecular Human Reproduction|April 4, 2017
Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidyAlexandra L Nguyen, Diego Marin, Anbo Zhou, et al.
Plos Genetics|April 28, 2016
A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic DefectsJinglan Zhang, Véronik Lachance, Adam Schaffner, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Genomics|January 28, 2012
Development of TaqMan allelic discrimination based genotyping of large DNA deletionsAnastasia Fedick, Jing Su, Nathan R Treff
BMC Research Notes|October 23, 2012
High-throughput real-time PCR-based genotyping without DNA purificationAnastasia Fedick, Jing Su, Chaim Jalas, et al.
Fertility and Sterility|January 15, 2013
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic diseaseNathan R Treff, Anastasia Fedick, Xin Tao, et al.
Plos One|April 5, 2013
High-throughput carrier screening using TaqMan allelic discriminationAnastasia Fedick, Jing Su, Chaim Jalas, et al.
The Journal of Molecular Diagnostics : JMD|January 17, 2016
Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk AssessmentJinglan Zhang, Anastasia Fedick, Stephanie Wasserman, et al.
Journal of Medical Genetics|September 14, 2013
Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposisSimon Edvardson, Angel Ashikov, Chaim Jalas, et al.
Journal of Medical Genetics|January 22, 2016
Deficiency of the alkaline ceramidase ACER3 manifests in early childhood by progressive leukodystrophySimon Edvardson, Jae Kyo Yi, Chaim Jalas, et al.
Molecular Human Reproduction|April 4, 2017
Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidyAlexandra L Nguyen, Diego Marin, Anbo Zhou, et al.
Plos Genetics|April 28, 2016
A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic DefectsJinglan Zhang, Véronik Lachance, Adam Schaffner, et al.
Pageof 1