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Elizabeth A Varga

Showing results (1-10 of 16) with videos related to

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Journal of Thrombosis and Thrombolysis|October 24, 2007
Genetics in the context of thrombophiliaElizabeth A Varga
Journal of Genetic Counseling|April 12, 2012
You want to do what? My mother's choice to have direct-to-consumer genetic testingElizabeth A Varga
Journal of Thrombosis and Thrombolysis|October 24, 2007
Genetic counseling for inherited thrombophiliasElizabeth A Varga
Seminars in Thrombosis and Hemostasis|December 17, 2008
Social and ethical controversies in thrombophilia testing and update on genetic risk factors for venous thromboembolismElizabeth A Varga, Bryce A Kerlin, Mark W Wurster
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2009
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephalyElizabeth A Varga, Matthew Pastore, Thomas Prior, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 10, 2010
Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephalyKim L McBride, Elizabeth A Varga, Matthew T Pastore, et al.
Cancer Investigation|July 17, 2015
Deep vein thrombosis (DVT) and pulmonary embolism (PE): awareness and prophylaxis practices reported by patients with cancerAnita Aggarwal, Lisa Fullam, Alan P Brownstein, et al.
Molecular Genetics & Genomic Medicine|September 17, 2020
Direct-to-consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the consumer experienceSarah L Elson, Nicholas A Furlotte, Bethann S Hromatka, et al.
Journal of Genetic Counseling|June 17, 2005
Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic CounselorsMercy Y Laurino, Robin L Bennett, Devki S Saraiya, et al.
Clinical Immunology (Orlando, Fla.)|May 11, 2024
A novel IKZF1 variant in a family with autosomal dominant CVID: A case for expanding exon coverage in inborn errors of immunityIvana Stojkic, Benjamin T Prince, Hye Sun Kuehn, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Thrombosis and Thrombolysis|October 24, 2007
Genetics in the context of thrombophiliaElizabeth A Varga
Journal of Genetic Counseling|April 12, 2012
You want to do what? My mother's choice to have direct-to-consumer genetic testingElizabeth A Varga
Journal of Thrombosis and Thrombolysis|October 24, 2007
Genetic counseling for inherited thrombophiliasElizabeth A Varga
Seminars in Thrombosis and Hemostasis|December 17, 2008
Social and ethical controversies in thrombophilia testing and update on genetic risk factors for venous thromboembolismElizabeth A Varga, Bryce A Kerlin, Mark W Wurster
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2009
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephalyElizabeth A Varga, Matthew Pastore, Thomas Prior, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 10, 2010
Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephalyKim L McBride, Elizabeth A Varga, Matthew T Pastore, et al.
Cancer Investigation|July 17, 2015
Deep vein thrombosis (DVT) and pulmonary embolism (PE): awareness and prophylaxis practices reported by patients with cancerAnita Aggarwal, Lisa Fullam, Alan P Brownstein, et al.
Molecular Genetics & Genomic Medicine|September 17, 2020
Direct-to-consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the consumer experienceSarah L Elson, Nicholas A Furlotte, Bethann S Hromatka, et al.
Journal of Genetic Counseling|June 17, 2005
Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic CounselorsMercy Y Laurino, Robin L Bennett, Devki S Saraiya, et al.
Clinical Immunology (Orlando, Fla.)|May 11, 2024
A novel IKZF1 variant in a family with autosomal dominant CVID: A case for expanding exon coverage in inborn errors of immunityIvana Stojkic, Benjamin T Prince, Hye Sun Kuehn, et al.
Pageof 2