Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Martin Delatycki

Showing results (11-20 of 57) with videos related to

Pageof 6
Sort By:
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|April 29, 2010
Dysarthria in Friedreich's ataxia: a perceptual analysisJoanne Folker, Bruce Murdoch, Louise Cahill, et al.
Neuropsychologia|September 22, 2009
Disruption to higher order processes in Friedreich ataxiaJoanne Fielding, Louise Corben, Phillip Cremer, et al.
Australian Journal of General Practice|December 18, 2024
Offering reproductive genetic carrier screening for cystic fibrosis, spinal muscular atrophy and fragile X syndrome: Views of Victorian general practitionersRuth Leibowitz, Sharon Lewis, Martin Delatycki, et al.
Neurology. Genetics|September 1, 2022
<i>RFC1</i>-Related Disease: Molecular and Clinical InsightsKayli Davies, David J Szmulewicz, Louise A Corben, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
An audit of clinical service examining the uptake of genetic testing by at-risk family membersLaura Forrest, Martin Delatycki, Lisette Curnow, et al.
Clinical Linguistics & Phonetics|January 27, 2010
Automatic method of pause measurement for normal and dysarthric speechKristin Rosen, Bruce Murdoch, Joanne Folker, et al.
Australian Journal of Primary Health|October 3, 2022
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome and spinal muscular atrophy: patterns of community and healthcare provider participation in a Victorian screening programRuth Leibowitz, Sharon Lewis, Jon Emery, et al.
AJOB Empirical Bioethics|September 30, 2017
How should we deal with misattributed paternity? A survey of lay public attitudesGeorgia Lowe, Jonathan Pugh, Guy Kahane, et al.
Journal of Child Neurology|December 21, 2019
False Negative Carrier Screening in Spinal Muscular AtrophySophie Butcher, Melanie Smith, Ian R Woodcock, et al.
The Medical Journal of Australia|December 13, 2012
Tay Sachs disease in Australia: reduced disease incidence despite stable carrier frequency in Australian JewsRaelia M Lew, Anne L Proos, Leslie Burnett, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|April 29, 2010
Dysarthria in Friedreich's ataxia: a perceptual analysisJoanne Folker, Bruce Murdoch, Louise Cahill, et al.
Neuropsychologia|September 22, 2009
Disruption to higher order processes in Friedreich ataxiaJoanne Fielding, Louise Corben, Phillip Cremer, et al.
Australian Journal of General Practice|December 18, 2024
Offering reproductive genetic carrier screening for cystic fibrosis, spinal muscular atrophy and fragile X syndrome: Views of Victorian general practitionersRuth Leibowitz, Sharon Lewis, Martin Delatycki, et al.
Neurology. Genetics|September 1, 2022
<i>RFC1</i>-Related Disease: Molecular and Clinical InsightsKayli Davies, David J Szmulewicz, Louise A Corben, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
An audit of clinical service examining the uptake of genetic testing by at-risk family membersLaura Forrest, Martin Delatycki, Lisette Curnow, et al.
Clinical Linguistics & Phonetics|January 27, 2010
Automatic method of pause measurement for normal and dysarthric speechKristin Rosen, Bruce Murdoch, Joanne Folker, et al.
Australian Journal of Primary Health|October 3, 2022
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome and spinal muscular atrophy: patterns of community and healthcare provider participation in a Victorian screening programRuth Leibowitz, Sharon Lewis, Jon Emery, et al.
AJOB Empirical Bioethics|September 30, 2017
How should we deal with misattributed paternity? A survey of lay public attitudesGeorgia Lowe, Jonathan Pugh, Guy Kahane, et al.
Journal of Child Neurology|December 21, 2019
False Negative Carrier Screening in Spinal Muscular AtrophySophie Butcher, Melanie Smith, Ian R Woodcock, et al.
The Medical Journal of Australia|December 13, 2012
Tay Sachs disease in Australia: reduced disease incidence despite stable carrier frequency in Australian JewsRaelia M Lew, Anne L Proos, Leslie Burnett, et al.
Pageof 6