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Meredith A Weaver

Showing results (1-10 of 11) with videos related to

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The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|November 25, 2003
A pilot survey on the licensing of DNA inventionsMichelle R Henry, Mildred K Cho, Meredith A Weaver, et al.
Science (New York, N.Y.)|August 24, 2002
Genetics. DNA patenting and licensingMichelle R Henry, Mildred K Cho, Meredith A Weaver, et al.
The Journal of Molecular Diagnostics : JMD|January 29, 2003
Effects of patents and licenses on the provision of clinical genetic testing servicesMildred K Cho, Samantha Illangasekare, Meredith A Weaver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2010
Medical foods: inborn errors of metabolism and the reimbursement dilemmaMeredith A Weaver, Alissa Johnson, Rani H Singh, et al.
Journal of Genetic Counseling|September 14, 2016
The Dynamics of a Genetic Counseling Peer Supervision GroupKatie L Lewis, Lori A H Erby, Amanda L Bergner, et al.
Molecular Genetics and Metabolism|August 11, 2019
Assessing the strength of evidence for genes implicated in fatty acid oxidation disorders using the ClinGen clinical validity frameworkJennifer L McGlaughon, Marzia Pasquali, Kathleen Wallace, et al.
Molecular Genetics and Metabolism|August 7, 2023
Specifications of the ACMG/AMP guidelines for ACADVL variant interpretationMay Flowers, Alexa Dickson, Marcus J Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2018
Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the futureLaura V Milko, Birgit H Funke, Ray E Hershberger, et al.
Human Mutation|October 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase GeneDiane B Zastrow, Heather Baudet, Wei Shen, et al.
Human Mutation|October 13, 2018
ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretationEdgar A Rivera-Muñoz, Laura V Milko, Steven M Harrison, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|November 25, 2003
A pilot survey on the licensing of DNA inventionsMichelle R Henry, Mildred K Cho, Meredith A Weaver, et al.
Science (New York, N.Y.)|August 24, 2002
Genetics. DNA patenting and licensingMichelle R Henry, Mildred K Cho, Meredith A Weaver, et al.
The Journal of Molecular Diagnostics : JMD|January 29, 2003
Effects of patents and licenses on the provision of clinical genetic testing servicesMildred K Cho, Samantha Illangasekare, Meredith A Weaver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2010
Medical foods: inborn errors of metabolism and the reimbursement dilemmaMeredith A Weaver, Alissa Johnson, Rani H Singh, et al.
Journal of Genetic Counseling|September 14, 2016
The Dynamics of a Genetic Counseling Peer Supervision GroupKatie L Lewis, Lori A H Erby, Amanda L Bergner, et al.
Molecular Genetics and Metabolism|August 11, 2019
Assessing the strength of evidence for genes implicated in fatty acid oxidation disorders using the ClinGen clinical validity frameworkJennifer L McGlaughon, Marzia Pasquali, Kathleen Wallace, et al.
Molecular Genetics and Metabolism|August 7, 2023
Specifications of the ACMG/AMP guidelines for ACADVL variant interpretationMay Flowers, Alexa Dickson, Marcus J Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2018
Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the futureLaura V Milko, Birgit H Funke, Ray E Hershberger, et al.
Human Mutation|October 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase GeneDiane B Zastrow, Heather Baudet, Wei Shen, et al.
Human Mutation|October 13, 2018
ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretationEdgar A Rivera-Muñoz, Laura V Milko, Steven M Harrison, et al.
Pageof 2