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Sarah Sandaradura

Showing results (1-10 of 7) with videos related to

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Oncotarget|September 5, 2015
LMOD3: the "missing link" in nemaline myopathy?Sarah Sandaradura, Kathryn N North
Journal of Paediatrics and Child Health|February 3, 2025
Navigating an Uninformative Genomic Test Result: A Practical GuideLaura St Clair, Claire Wong, Christopher Elliot, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2024
A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capabilityGiulia McCorkell, Amy Nisselle, Donna Halton, et al.
American Journal of Human Genetics|September 7, 2019
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
American Journal of Human Genetics|May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
The Journal of Molecular Diagnostics : JMD|May 7, 2021
Clinically Responsive Genomic Analysis Pipelines: Elements to Improve Detection Rate and EfficiencySamantha Leigh Sundercombe, Marina Berbic, Carey-Anne Evans, et al.
Human Mutation|September 17, 2013
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformationNicole Revencu, Laurence M Boon, Antonella Mendola, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Oncotarget|September 5, 2015
LMOD3: the "missing link" in nemaline myopathy?Sarah Sandaradura, Kathryn N North
Journal of Paediatrics and Child Health|February 3, 2025
Navigating an Uninformative Genomic Test Result: A Practical GuideLaura St Clair, Claire Wong, Christopher Elliot, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2024
A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capabilityGiulia McCorkell, Amy Nisselle, Donna Halton, et al.
American Journal of Human Genetics|September 7, 2019
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
American Journal of Human Genetics|May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
The Journal of Molecular Diagnostics : JMD|May 7, 2021
Clinically Responsive Genomic Analysis Pipelines: Elements to Improve Detection Rate and EfficiencySamantha Leigh Sundercombe, Marina Berbic, Carey-Anne Evans, et al.
Human Mutation|September 17, 2013
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformationNicole Revencu, Laurence M Boon, Antonella Mendola, et al.
Pageof 1