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David J Amor

Showing results (51-60 of 275) with videos related to

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Brain : a Journal of Neurology|June 28, 2019
IREB2-associated neurodegenerationMonica S Cooper, Zornitza Stark, Sebastian Lunke, et al.
American Journal of Medical Genetics. Part A|May 7, 2016
"I'm Healthy, It's Not Going To Be Me": Exploring experiences of carriers identified through a population reproductive genetic carrier screening panel in AustraliaCatherine A Beard, David J Amor, Louisa Di Pietro, et al.
Child: Care, Health and Development|April 1, 2024
Hypotonic cerebral palsyMonica S Cooper, Giuliana C Antolovich, Michael C Fahey, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Lambdoid synostosis and craniofacial dysmorphism with normal intellect: A novel syndrome?Claudine Rieubland, Anthony D Holmes, Melody Caramins, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practiceGemma R Brett, Sylvia A Metcalfe, David J Amor, et al.
European Journal of Medical Genetics|July 31, 2010
De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic featuresZornitza Stark, Damien L Bruno, Hayley Mountford, et al.
Molecular Genetics and Metabolism|March 1, 2024
The Mendelian disorders of chromatin machinery: Harnessing metabolic pathways and therapies for treatmentSarah Donoghue, Jordan Wright, Anne K Voss, et al.
The Laryngoscope|December 31, 2020
Exome Sequencing for Isolated Congenital Hearing Loss: A Cost-Effectiveness AnalysisLilian Downie, David J Amor, Jane Halliday, et al.
The Medical Journal of Australia|March 16, 2011
A case for cystic fibrosis carrier testing in the general populationBelinda J McClaren, Sylvia A Metcalfe, David J Amor, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|September 15, 2023
An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of SpeechMariana L Lauretta, Anna Jarmolowicz, David J Amor, et al.
Pageof 28

Showing results (51-60 of 275) with videos related to

Sort By:
Pageof 28
Brain : a Journal of Neurology|June 28, 2019
IREB2-associated neurodegenerationMonica S Cooper, Zornitza Stark, Sebastian Lunke, et al.
American Journal of Medical Genetics. Part A|May 7, 2016
"I'm Healthy, It's Not Going To Be Me": Exploring experiences of carriers identified through a population reproductive genetic carrier screening panel in AustraliaCatherine A Beard, David J Amor, Louisa Di Pietro, et al.
Child: Care, Health and Development|April 1, 2024
Hypotonic cerebral palsyMonica S Cooper, Giuliana C Antolovich, Michael C Fahey, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Lambdoid synostosis and craniofacial dysmorphism with normal intellect: A novel syndrome?Claudine Rieubland, Anthony D Holmes, Melody Caramins, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practiceGemma R Brett, Sylvia A Metcalfe, David J Amor, et al.
European Journal of Medical Genetics|July 31, 2010
De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic featuresZornitza Stark, Damien L Bruno, Hayley Mountford, et al.
Molecular Genetics and Metabolism|March 1, 2024
The Mendelian disorders of chromatin machinery: Harnessing metabolic pathways and therapies for treatmentSarah Donoghue, Jordan Wright, Anne K Voss, et al.
The Laryngoscope|December 31, 2020
Exome Sequencing for Isolated Congenital Hearing Loss: A Cost-Effectiveness AnalysisLilian Downie, David J Amor, Jane Halliday, et al.
The Medical Journal of Australia|March 16, 2011
A case for cystic fibrosis carrier testing in the general populationBelinda J McClaren, Sylvia A Metcalfe, David J Amor, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|September 15, 2023
An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of SpeechMariana L Lauretta, Anna Jarmolowicz, David J Amor, et al.
Pageof 28