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

Christopher A Tan

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Developmental Disabilities Research Reviews|March 27, 2012
Expanding newborn screening for lysosomal disorders: opportunities and challengesDarrel J Waggoner, Christopher A Tan
Frontiers in Genetics|March 26, 2016
An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case ReportStephanie A Cohen, Christopher A Tan, Ryan Bisson
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|October 7, 2005
Percutaneous closure of perimembranous ventricular septal defect associated with a ventricular septal aneurysm using the Amplatzer ductal occluderChristopher A Tan, Daniel S Levi, John W Moore
BMC Pediatrics|March 18, 2023
Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case reportVivien Phung, Kathryn E Singh, Saar Danon, et al.
Brain & Development|June 4, 2013
The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencingChristopher A Tan, Scott Topper, Catherine Ward Melver, et al.
Genetic Testing and Molecular Biomarkers|July 30, 2020
Incorporating Spinal Muscular Atrophy Analysis by Next-Generation Sequencing into a Comprehensive Multigene Panel for Neuromuscular DisordersChristopher A Tan, Marjorie Jody Westbrook, Rebecca Truty, et al.
American Journal of Medical Genetics. Part A|March 10, 2016
Autosomal recessive MFN2-related Charcot-Marie-Tooth disease with diaphragmatic weakness: Case report and literature reviewChristopher A Tan, Marina Rabideau, Amy Blevins, et al.
Molecular Genetics & Genomic Medicine|September 7, 2019
A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathyJennifer Roggenbuck, Kelly Rich, Ana Morales, et al.
Frontiers in Neurology|May 24, 2021
SMA Identified: Clinical and Molecular Findings From a Sponsored Testing Program for Spinal Muscular Atrophy in More Than 2,000 IndividualsB Monica Bowen, Rebecca Truty, Swaroop Aradhya, et al.
Neurology. Genetics|April 28, 2020
Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disordersThomas L Winder, Christopher A Tan, Sarah Klemm, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Developmental Disabilities Research Reviews|March 27, 2012
Expanding newborn screening for lysosomal disorders: opportunities and challengesDarrel J Waggoner, Christopher A Tan
Frontiers in Genetics|March 26, 2016
An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case ReportStephanie A Cohen, Christopher A Tan, Ryan Bisson
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|October 7, 2005
Percutaneous closure of perimembranous ventricular septal defect associated with a ventricular septal aneurysm using the Amplatzer ductal occluderChristopher A Tan, Daniel S Levi, John W Moore
BMC Pediatrics|March 18, 2023
Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case reportVivien Phung, Kathryn E Singh, Saar Danon, et al.
Brain & Development|June 4, 2013
The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencingChristopher A Tan, Scott Topper, Catherine Ward Melver, et al.
Genetic Testing and Molecular Biomarkers|July 30, 2020
Incorporating Spinal Muscular Atrophy Analysis by Next-Generation Sequencing into a Comprehensive Multigene Panel for Neuromuscular DisordersChristopher A Tan, Marjorie Jody Westbrook, Rebecca Truty, et al.
American Journal of Medical Genetics. Part A|March 10, 2016
Autosomal recessive MFN2-related Charcot-Marie-Tooth disease with diaphragmatic weakness: Case report and literature reviewChristopher A Tan, Marina Rabideau, Amy Blevins, et al.
Molecular Genetics & Genomic Medicine|September 7, 2019
A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathyJennifer Roggenbuck, Kelly Rich, Ana Morales, et al.
Frontiers in Neurology|May 24, 2021
SMA Identified: Clinical and Molecular Findings From a Sponsored Testing Program for Spinal Muscular Atrophy in More Than 2,000 IndividualsB Monica Bowen, Rebecca Truty, Swaroop Aradhya, et al.
Neurology. Genetics|April 28, 2020
Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disordersThomas L Winder, Christopher A Tan, Sarah Klemm, et al.
Pageof 2