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Zornitza Stark

Showing results (101-110 of 270) with videos related to

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Nephrology (Carlton, Vic.)|September 22, 2018
Renal genetics in Australia: Kidney medicine in the genomic ageKushani Jayasinghe, Catherine Quinlan, Zornitza Stark, et al.
The New England Journal of Medicine|June 5, 2014
Clinical problem-solving. Spot diagnosisZornitza Stark, Lynda J Campbell, Catherine Mitchell, et al.
NPJ Genomic Medicine|October 22, 2022
Co-design, implementation, and evaluation of plain language genomic test reportsGemma R Brett, Aisha Ward, Sophie E Bouffler, 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.
Journal of Paediatrics and Child Health|February 14, 2019
Diagnostic and service impact of genomic testing technologies in a neonatal intensive care unitNatalie B Tan, Tiong Yang Tan, Melissa M Martyn, et al.
Journal of Human Genetics|March 3, 2017
ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndromeSatoko Miyatake, Nobuhiko Okamoto, Zornitza Stark, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?Jan M Friedman, Yvonne Bombard, Martina C Cornel, et al.
Human Mutation|August 28, 2015
Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1Michael P Guy, Marie Shaw, Catherine L Weiner, et al.
Frontiers in Medicine|June 20, 2022
The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown AetiologyJacqueline Soraru, Sadia Jahan, Catherine Quinlan, et al.
Nature Medicine|June 19, 2024
Exploring the benefits, harms and costs of genomic newborn screening for rare diseasesEmma L Baple, Richard H Scott, Siddharth Banka, et al.
Pageof 27

Showing results (101-110 of 270) with videos related to

Sort By:
Pageof 27
Nephrology (Carlton, Vic.)|September 22, 2018
Renal genetics in Australia: Kidney medicine in the genomic ageKushani Jayasinghe, Catherine Quinlan, Zornitza Stark, et al.
The New England Journal of Medicine|June 5, 2014
Clinical problem-solving. Spot diagnosisZornitza Stark, Lynda J Campbell, Catherine Mitchell, et al.
NPJ Genomic Medicine|October 22, 2022
Co-design, implementation, and evaluation of plain language genomic test reportsGemma R Brett, Aisha Ward, Sophie E Bouffler, 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.
Journal of Paediatrics and Child Health|February 14, 2019
Diagnostic and service impact of genomic testing technologies in a neonatal intensive care unitNatalie B Tan, Tiong Yang Tan, Melissa M Martyn, et al.
Journal of Human Genetics|March 3, 2017
ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndromeSatoko Miyatake, Nobuhiko Okamoto, Zornitza Stark, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?Jan M Friedman, Yvonne Bombard, Martina C Cornel, et al.
Human Mutation|August 28, 2015
Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1Michael P Guy, Marie Shaw, Catherine L Weiner, et al.
Frontiers in Medicine|June 20, 2022
The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown AetiologyJacqueline Soraru, Sadia Jahan, Catherine Quinlan, et al.
Nature Medicine|June 19, 2024
Exploring the benefits, harms and costs of genomic newborn screening for rare diseasesEmma L Baple, Richard H Scott, Siddharth Banka, et al.
Pageof 27