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Christine E Miller

Showing results (11-20 of 24) with videos related to

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American Journal of Medical Genetics. Part A|March 26, 2014
Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testingChristine E Miller, Patti Krautscheid, Erin E Baldwin, et al.
Journal of Fungi (Basel, Switzerland)|August 28, 2024
A <i>Fusarium verticillioides MAT1-2</i> Strain near Isogenic to the Sequenced FGSC7600 Strain for Producing Homozygous Multigene MutantsScott E Gold, Daren W Brown, Felicia N Williams, et al.
Human Mutation|March 6, 2010
Clinical analysis of PMS2: mutation detection and avoidance of pseudogenesCecily P Vaughn, Jorge Robles, Jeffrey J Swensen, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Implementation of a cost-effective unlabeled probe high-resolution melt assay for genotyping of Factor V LeidenAnnika M Svensson, Lan-Szu Chou, Cindy Meadows, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Detection of large rearrangements in the cystic fibrosis transmembrane conductance regulator gene by multiplex ligation-dependent probe amplification assay when sequencing fails to detect two disease-causing mutationsAnnika M Svensson, Lan-Szu Chou, Christine E Miller, et al.
Clinical Case Reports|December 20, 2018
Novel mutation in <i>CCBE 1</i> as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1Dora J Melber, Tara S Andreasen, Rong Mao, et al.
Neurology. Genetics|April 14, 2023
<i>SON</i>-Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine: Putative Role of <i>PRRT2</i>Jordan Langford, Lana Vukadin, John C Carey, et al.
Children (Basel, Switzerland)|June 28, 2023
Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill InfantsJoseph Reiley, Pablo Botas, Christine E Miller, et al.
The Journal of Molecular Diagnostics : JMD|February 17, 2015
Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular PathologyMadhuri Hegde, Sherri Bale, Pinar Bayrak-Toydemir, et al.
Journal of Food Protection|February 11, 2022
Survey of Meat Collected from Commercial Broiler Processing Plants Suggests Low Levels of Semicarbazide Can Be Created during Immersion ChillingTrevor R Mitchell, Mark E Berrang, Scott E Gold, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|March 26, 2014
Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testingChristine E Miller, Patti Krautscheid, Erin E Baldwin, et al.
Journal of Fungi (Basel, Switzerland)|August 28, 2024
A <i>Fusarium verticillioides MAT1-2</i> Strain near Isogenic to the Sequenced FGSC7600 Strain for Producing Homozygous Multigene MutantsScott E Gold, Daren W Brown, Felicia N Williams, et al.
Human Mutation|March 6, 2010
Clinical analysis of PMS2: mutation detection and avoidance of pseudogenesCecily P Vaughn, Jorge Robles, Jeffrey J Swensen, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Implementation of a cost-effective unlabeled probe high-resolution melt assay for genotyping of Factor V LeidenAnnika M Svensson, Lan-Szu Chou, Cindy Meadows, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Detection of large rearrangements in the cystic fibrosis transmembrane conductance regulator gene by multiplex ligation-dependent probe amplification assay when sequencing fails to detect two disease-causing mutationsAnnika M Svensson, Lan-Szu Chou, Christine E Miller, et al.
Clinical Case Reports|December 20, 2018
Novel mutation in <i>CCBE 1</i> as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1Dora J Melber, Tara S Andreasen, Rong Mao, et al.
Neurology. Genetics|April 14, 2023
<i>SON</i>-Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine: Putative Role of <i>PRRT2</i>Jordan Langford, Lana Vukadin, John C Carey, et al.
Children (Basel, Switzerland)|June 28, 2023
Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill InfantsJoseph Reiley, Pablo Botas, Christine E Miller, et al.
The Journal of Molecular Diagnostics : JMD|February 17, 2015
Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular PathologyMadhuri Hegde, Sherri Bale, Pinar Bayrak-Toydemir, et al.
Journal of Food Protection|February 11, 2022
Survey of Meat Collected from Commercial Broiler Processing Plants Suggests Low Levels of Semicarbazide Can Be Created during Immersion ChillingTrevor R Mitchell, Mark E Berrang, Scott E Gold, et al.
Pageof 3