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European Journal of Human Genetics : EJHG
|
October 20, 2023
Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia
Danya F Vears, Fiona Lynch, Amy Nisselle, et al.
Pediatrics
|
January 3, 2019
Rapid Challenges: Ethics and Genomic Neonatal Intensive Care
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, et al.
Biology of Reproduction
|
July 31, 2022
Genomic testing in premature ovarian insufficiency: proceed with caution
Elena J Tucker, Tiong Y Tan, Zornitza Stark, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 9, 2024
Determining priority indicators of utility for genomic testing in rare disease: A Delphi study
Zoe Fehlberg, Ilias Goranitis, Andrew J Mallett, et al.
European Journal of Human Genetics : EJHG
|
February 18, 2011
Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring
Zornitza Stark, Rebecca Storen, Bruce Bennetts, et al.
Journal of Medical Ethics
|
June 10, 2016
Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?
Zornitza Stark, Jane Wallace, Lynn Gillam, et al.
European Journal of Human Genetics : EJHG
|
August 11, 2022
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
Fiona Lynch, Amy Nisselle, Zornitza Stark, et al.
European Journal of Human Genetics : EJHG
|
August 24, 2021
Parents' experiences of decision making for rapid genomic sequencing in intensive care
Fiona Lynch, Amy Nisselle, Zornitza Stark, et al.
Brain : a Journal of Neurology
|
June 28, 2019
IREB2-associated neurodegeneration
Monica S Cooper, Zornitza Stark, Sebastian Lunke, et al.
Human Genomics
|
August 8, 2023
The application of long-read sequencing in clinical settings
Josephine B Oehler, Helen Wright, Zornitza Stark, et al.
Page
of 27
Search research articles
Search
Showing results (41-50 of 270) with videos related to
Sort By:
Page
of 27
European Journal of Human Genetics : EJHG
|
October 20, 2023
Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia
Danya F Vears, Fiona Lynch, Amy Nisselle, et al.
Pediatrics
|
January 3, 2019
Rapid Challenges: Ethics and Genomic Neonatal Intensive Care
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, et al.
Biology of Reproduction
|
July 31, 2022
Genomic testing in premature ovarian insufficiency: proceed with caution
Elena J Tucker, Tiong Y Tan, Zornitza Stark, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 9, 2024
Determining priority indicators of utility for genomic testing in rare disease: A Delphi study
Zoe Fehlberg, Ilias Goranitis, Andrew J Mallett, et al.
European Journal of Human Genetics : EJHG
|
February 18, 2011
Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring
Zornitza Stark, Rebecca Storen, Bruce Bennetts, et al.
Journal of Medical Ethics
|
June 10, 2016
Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?
Zornitza Stark, Jane Wallace, Lynn Gillam, et al.
European Journal of Human Genetics : EJHG
|
August 11, 2022
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
Fiona Lynch, Amy Nisselle, Zornitza Stark, et al.
European Journal of Human Genetics : EJHG
|
August 24, 2021
Parents' experiences of decision making for rapid genomic sequencing in intensive care
Fiona Lynch, Amy Nisselle, Zornitza Stark, et al.
Brain : a Journal of Neurology
|
June 28, 2019
IREB2-associated neurodegeneration
Monica S Cooper, Zornitza Stark, Sebastian Lunke, et al.
Human Genomics
|
August 8, 2023
The application of long-read sequencing in clinical settings
Josephine B Oehler, Helen Wright, Zornitza Stark, et al.
Page
of 27