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Nursing Standard (Royal College of Nursing (Great Britain) : 1987)
|
November 3, 2009
Get ready for the journey
Naomi Baker
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)
|
June 2, 2009
Ready to register
Naomi Baker
Current Rheumatology Reports
|
December 17, 2013
The collagenopathies: review of clinical phenotypes and molecular correlations
Rebekah Jobling, Rohan D'Souza, Naomi Baker, et al.
European Journal of Human Genetics : EJHG
|
February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in Australia
Megan 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 practice
Ingrid 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 malformations
Daniz 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 interpretation
Emma Tudini, James Andrews, David M Lawrence, et al.
Nature Genetics
|
October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
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Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)
|
November 3, 2009
Get ready for the journey
Naomi Baker
Nursing Standard (Royal College of Nursing (Great Britain) : 1987)
|
June 2, 2009
Ready to register
Naomi Baker
Current Rheumatology Reports
|
December 17, 2013
The collagenopathies: review of clinical phenotypes and molecular correlations
Rebekah Jobling, Rohan D'Souza, Naomi Baker, et al.
European Journal of Human Genetics : EJHG
|
February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in Australia
Megan 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 practice
Ingrid 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 malformations
Daniz 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 interpretation
Emma Tudini, James Andrews, David M Lawrence, et al.
Nature Genetics
|
October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
Page
of 1