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

V Reid Sutton

Showing results (21-30 of 184) with videos related to

Pageof 19
Sort By:
American Journal of Medical Genetics. Part A|October 18, 2008
Neuroimaging aspects of Aicardi syndromeBobbi Hopkins, V Reid Sutton, Richard Alan Lewis, et al.
Orthodontics & Craniofacial Research|August 29, 2023
Cranio-cervical abnormalities in moderate-to-severe osteogenesis imperfecta - Genotypic and phenotypic determinantsJuliana Marulanda, Jean-Marc Retrouvey, Brendan Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2012
The development and implementation of an in-service exam for medical genetics residency programsNathaniel H Robin, V Reid Sutton, John Caldwell, et al.
Molecular Genetics and Metabolism|January 4, 2022
Perceptions and use of phenylbutyrate metabolite testing in urea cycle disorders: Results of a clinician survey and analysis of a centralized testing databaseCan Ficicioglu, Ning Liu, Qin Sun, et al.
American Journal of Medical Genetics|September 20, 2002
Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short armsV Reid Sutton, Karen J Coveler, Seema R Lalani, et al.
American Journal of Perinatology|May 12, 2010
Management of ornithine transcarbamylase deficiency in pregnancyHector Mendez-Figueroa, Kerri Lamance, V Reid Sutton, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
A dominantly inherited spondylometaphyseal dysplasia with "corner fractures" and congenital scoliosisV Reid Sutton, James C Hyland, William A Phillips, et al.
Bone|August 15, 2022
Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAPJuliana Marulanda, Karissa Ludwig, Francis Glorieux, et al.
Molecular Genetics and Metabolism|October 14, 2025
Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs)Xueyang Pan, Yue Wang, Ning Liu, et al.
Bone|July 31, 2020
Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profilesDamian Rauch, Marie-Eve Robinson, Cristian Seiltgens, et al.
Pageof 19

Showing results (21-30 of 184) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics. Part A|October 18, 2008
Neuroimaging aspects of Aicardi syndromeBobbi Hopkins, V Reid Sutton, Richard Alan Lewis, et al.
Orthodontics & Craniofacial Research|August 29, 2023
Cranio-cervical abnormalities in moderate-to-severe osteogenesis imperfecta - Genotypic and phenotypic determinantsJuliana Marulanda, Jean-Marc Retrouvey, Brendan Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2012
The development and implementation of an in-service exam for medical genetics residency programsNathaniel H Robin, V Reid Sutton, John Caldwell, et al.
Molecular Genetics and Metabolism|January 4, 2022
Perceptions and use of phenylbutyrate metabolite testing in urea cycle disorders: Results of a clinician survey and analysis of a centralized testing databaseCan Ficicioglu, Ning Liu, Qin Sun, et al.
American Journal of Medical Genetics|September 20, 2002
Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short armsV Reid Sutton, Karen J Coveler, Seema R Lalani, et al.
American Journal of Perinatology|May 12, 2010
Management of ornithine transcarbamylase deficiency in pregnancyHector Mendez-Figueroa, Kerri Lamance, V Reid Sutton, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
A dominantly inherited spondylometaphyseal dysplasia with "corner fractures" and congenital scoliosisV Reid Sutton, James C Hyland, William A Phillips, et al.
Bone|August 15, 2022
Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAPJuliana Marulanda, Karissa Ludwig, Francis Glorieux, et al.
Molecular Genetics and Metabolism|October 14, 2025
Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs)Xueyang Pan, Yue Wang, Ning Liu, et al.
Bone|July 31, 2020
Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profilesDamian Rauch, Marie-Eve Robinson, Cristian Seiltgens, et al.
Pageof 19