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Naomi Baker

Showing results (1-10 of 8) with videos related to

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Nursing Standard (Royal College of Nursing (Great Britain) : 1987)|November 3, 2009
Get ready for the journeyNaomi Baker
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)|June 2, 2009
Ready to registerNaomi Baker
Current Rheumatology Reports|December 17, 2013
The collagenopathies: review of clinical phenotypes and molecular correlationsRebekah Jobling, Rohan D'Souza, Naomi Baker, et al.
European Journal of Human Genetics : EJHG|February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in AustraliaMegan Ball, Naomi Baker, Sze Chern Lim, et al.
Developmental Medicine and Child Neurology|June 14, 2022
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practiceIngrid E Scheffer, Caitlin A Bennett, Deepak Gill, et al.
Brain Communications|March 6, 2024
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformationsDaniz Kooshavar, David J Amor, Kirsten Boggs, et al.
American Journal of Human Genetics|November 4, 2022
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretationEmma Tudini, James Andrews, David M Lawrence, et al.
Nature Genetics|October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)|November 3, 2009
Get ready for the journeyNaomi Baker
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)|June 2, 2009
Ready to registerNaomi Baker
Current Rheumatology Reports|December 17, 2013
The collagenopathies: review of clinical phenotypes and molecular correlationsRebekah Jobling, Rohan D'Souza, Naomi Baker, et al.
European Journal of Human Genetics : EJHG|February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in AustraliaMegan Ball, Naomi Baker, Sze Chern Lim, et al.
Developmental Medicine and Child Neurology|June 14, 2022
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practiceIngrid E Scheffer, Caitlin A Bennett, Deepak Gill, et al.
Brain Communications|March 6, 2024
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformationsDaniz Kooshavar, David J Amor, Kirsten Boggs, et al.
American Journal of Human Genetics|November 4, 2022
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretationEmma Tudini, James Andrews, David M Lawrence, et al.
Nature Genetics|October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
Pageof 1