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

Robert B Wilson

Showing results (41-50 of 80) with videos related to

Pageof 8
Sort By:
Archives of Neurology|May 22, 2002
Friedreich ataxia: effects of genetic understanding on clinical evaluation and therapyDavid R Lynch, Jennifer M Farmer, Laura J Balcer, et al.
Gastrointestinal Endoscopy|May 26, 2007
A case of ischemic colitis associated with factor V Leiden mutation: successful treatment with anticoagulationBernard Wai Keat Chin, Darrilyn Greenberg, Robert B Wilson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2005
Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation testsShuji Ogino, Pamela Flodman, Robert B Wilson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 17, 2004
Bayesian analysis for cystic fibrosis risks in prenatal and carrier screeningShuji Ogino, Robert B Wilson, Bert Gold, et al.
Redox Biology|December 16, 2014
Insights into the role of oxidative stress in the pathology of Friedreich ataxia using peroxidation resistant polyunsaturated fatty acidsM Grazia Cotticelli, Andrew M Crabbe, Robert B Wilson, et al.
CNS Drugs|March 27, 2009
Pharmacotherapy for Friedreich ataxiaAmy Y Tsou, Lisa S Friedman, Robert B Wilson, et al.
The Journal of Molecular Diagnostics : JMD|January 26, 2007
Standard mutation nomenclature in molecular diagnostics: practical and educational challengesShuji Ogino, Margaret L Gulley, Johan T den Dunnen, et al.
Clinical Chemistry|January 11, 2025
A Multianalyte Machine Learning Model to Detect Wrong Blood in Complete Blood Count Tube Errors in a Pediatric SettingBrendan V Graham, Stephen R Master, Amrom E Obstfeld, et al.
The Journal of Molecular Diagnostics : JMD|January 14, 2011
Population carrier screening for spinal muscular atrophy a position statement of the association for molecular pathologyKasinathan Muralidharan, Robert B Wilson, Shuji Ogino, et al.
European Journal of Human Genetics : EJHG|April 4, 2003
Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1Shuji Ogino, Sizhen Gao, Debra G B Leonard, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Archives of Neurology|May 22, 2002
Friedreich ataxia: effects of genetic understanding on clinical evaluation and therapyDavid R Lynch, Jennifer M Farmer, Laura J Balcer, et al.
Gastrointestinal Endoscopy|May 26, 2007
A case of ischemic colitis associated with factor V Leiden mutation: successful treatment with anticoagulationBernard Wai Keat Chin, Darrilyn Greenberg, Robert B Wilson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2005
Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation testsShuji Ogino, Pamela Flodman, Robert B Wilson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 17, 2004
Bayesian analysis for cystic fibrosis risks in prenatal and carrier screeningShuji Ogino, Robert B Wilson, Bert Gold, et al.
Redox Biology|December 16, 2014
Insights into the role of oxidative stress in the pathology of Friedreich ataxia using peroxidation resistant polyunsaturated fatty acidsM Grazia Cotticelli, Andrew M Crabbe, Robert B Wilson, et al.
CNS Drugs|March 27, 2009
Pharmacotherapy for Friedreich ataxiaAmy Y Tsou, Lisa S Friedman, Robert B Wilson, et al.
The Journal of Molecular Diagnostics : JMD|January 26, 2007
Standard mutation nomenclature in molecular diagnostics: practical and educational challengesShuji Ogino, Margaret L Gulley, Johan T den Dunnen, et al.
Clinical Chemistry|January 11, 2025
A Multianalyte Machine Learning Model to Detect Wrong Blood in Complete Blood Count Tube Errors in a Pediatric SettingBrendan V Graham, Stephen R Master, Amrom E Obstfeld, et al.
The Journal of Molecular Diagnostics : JMD|January 14, 2011
Population carrier screening for spinal muscular atrophy a position statement of the association for molecular pathologyKasinathan Muralidharan, Robert B Wilson, Shuji Ogino, et al.
European Journal of Human Genetics : EJHG|April 4, 2003
Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1Shuji Ogino, Sizhen Gao, Debra G B Leonard, et al.
Pageof 8