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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 inventions
Michelle R Henry, Mildred K Cho, Meredith A Weaver, et al.
Science (New York, N.Y.)
|
August 24, 2002
Genetics. DNA patenting and licensing
Michelle 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 services
Mildred 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 dilemma
Meredith A Weaver, Alissa Johnson, Rani H Singh, et al.
Journal of Genetic Counseling
|
September 14, 2016
The Dynamics of a Genetic Counseling Peer Supervision Group
Katie 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 framework
Jennifer L McGlaughon, Marzia Pasquali, Kathleen Wallace, et al.
Molecular Genetics and Metabolism
|
August 7, 2023
Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation
May 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 future
Laura 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 Gene
Diane 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 interpretation
Edgar A Rivera-Muñoz, Laura V Milko, Steven M Harrison, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 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 inventions
Michelle R Henry, Mildred K Cho, Meredith A Weaver, et al.
Science (New York, N.Y.)
|
August 24, 2002
Genetics. DNA patenting and licensing
Michelle 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 services
Mildred 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 dilemma
Meredith A Weaver, Alissa Johnson, Rani H Singh, et al.
Journal of Genetic Counseling
|
September 14, 2016
The Dynamics of a Genetic Counseling Peer Supervision Group
Katie 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 framework
Jennifer L McGlaughon, Marzia Pasquali, Kathleen Wallace, et al.
Molecular Genetics and Metabolism
|
August 7, 2023
Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation
May 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 future
Laura 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 Gene
Diane 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 interpretation
Edgar A Rivera-Muñoz, Laura V Milko, Steven M Harrison, et al.
Page
of 2