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

Hope Northrup

Showing results (11-20 of 157) with videos related to

Pageof 16
Sort By:
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2015
Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotypeJaclyn E Ruggiero, Hope Northrup, Kit Sing Au
American Journal of Medical Genetics. Part A|April 11, 2003
Deletion 12q: a second patient with 12q24.31q24.32 deletionPamela L Plotner, Janice L Smith, Hope Northrup
American Journal of Medical Genetics. Part A|September 26, 2017
Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturnedKit Sing Au, Tina O Findley, Hope Northrup
Current Opinion in Pediatrics|November 14, 2008
Tuberous sclerosis complex: disease modifiers and treatmentsKit Sing Au, Catherine H Ward, Hope Northrup
Developmental Disabilities Research Reviews|April 27, 2010
Epidemiologic and genetic aspects of spina bifida and other neural tube defectsKit Sing Au, Allison Ashley-Koch, Hope Northrup
American Journal of Obstetrics and Gynecology|May 13, 2014
Genetic variations in the GLUT3 gene associated with myelomeningoceleBrendan D Connealy, Hope Northrup, Kit Sing Au
American Journal of Medical Genetics|July 19, 2002
Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literaturePamela L Plotner, Janice L Smith, Hope Northrup
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 30, 2011
Genetic studies of the cystathionine beta-synthase gene and myelomeningoceleMelissa M Tilley, Hope Northrup, Kit Sing Au
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 14, 2012
Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningoceleChiamaka N Aneji, Hope Northrup, Kit Sing Au
European Journal of Medical Genetics|April 1, 2017
Wiedemann-Steiner syndrome: Novel pathogenic variant and review of literatureAnjali Aggarwal, David F Rodriguez-Buritica, Hope Northrup
Pageof 16

Showing results (11-20 of 157) with videos related to

Sort By:
Pageof 16
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2015
Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotypeJaclyn E Ruggiero, Hope Northrup, Kit Sing Au
American Journal of Medical Genetics. Part A|April 11, 2003
Deletion 12q: a second patient with 12q24.31q24.32 deletionPamela L Plotner, Janice L Smith, Hope Northrup
American Journal of Medical Genetics. Part A|September 26, 2017
Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturnedKit Sing Au, Tina O Findley, Hope Northrup
Current Opinion in Pediatrics|November 14, 2008
Tuberous sclerosis complex: disease modifiers and treatmentsKit Sing Au, Catherine H Ward, Hope Northrup
Developmental Disabilities Research Reviews|April 27, 2010
Epidemiologic and genetic aspects of spina bifida and other neural tube defectsKit Sing Au, Allison Ashley-Koch, Hope Northrup
American Journal of Obstetrics and Gynecology|May 13, 2014
Genetic variations in the GLUT3 gene associated with myelomeningoceleBrendan D Connealy, Hope Northrup, Kit Sing Au
American Journal of Medical Genetics|July 19, 2002
Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literaturePamela L Plotner, Janice L Smith, Hope Northrup
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 30, 2011
Genetic studies of the cystathionine beta-synthase gene and myelomeningoceleMelissa M Tilley, Hope Northrup, Kit Sing Au
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 14, 2012
Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningoceleChiamaka N Aneji, Hope Northrup, Kit Sing Au
European Journal of Medical Genetics|April 1, 2017
Wiedemann-Steiner syndrome: Novel pathogenic variant and review of literatureAnjali Aggarwal, David F Rodriguez-Buritica, Hope Northrup
Pageof 16