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

Julie R Jones

Showing results (1-10 of 62) with videos related to

Pageof 7
Sort By:
Current Protocols in Human Genetics|February 11, 2014
Nonrandom X chromosome inactivation detectionJulie R Jones
American Journal of Medical Genetics. Part A|April 7, 2020
Fatal hyperkeratosis syndrome in four siblings due to dolichol kinase deficiencyBryan D Hall, Roger E Stevenson, Julie R Jones
Multiple Sclerosis and Related Disorders|May 12, 2018
Forkhead box C1 gene variant causing glaucoma and small vessel angiopathy can mimic multiple sclerosisJagannadha R Avasarala, Julie R Jones, Curtis R Rogers
Nutrition Reviews|February 24, 2006
Dietary reference intakes: implications for fiber labeling and consumption: a summary of the International Life Sciences Institute North America Fiber Workshop, June 1-2, 2004, Washington, DCJulie R Jones, David M Lineback, Marci J Levine
Methods in Molecular Medicine|November 16, 2004
Strategies for the use of site-specific recombinases in genome engineeringJulie R Jones, Kathy D Shelton, Mark A Magnuson
Journal of Inherited Metabolic Disease|September 15, 2012
Molecular characterization of 355 mucopolysaccharidosis patients reveals 104 novel mutationsLaura M Pollard, Julie R Jones, Tim C Wood
European Journal of Medical Genetics|February 28, 2016
CHD8 intragenic deletion associated with autism spectrum disorderElliot S Stolerman, Brooke Smith, Alka Chaubey, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Classic phenotype of Coffin-Lowry syndrome in a female with stimulus-induced drop episodes and a genotype with preserved N-terminal kinase domainKitiwan Rojnueangnit, Julie R Jones, Monica J Basehore, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 14, 2018
Ovotesticular Disorder of Sex Development (Ovotestis) in Simpson-Golabi-Behmel Syndrome: Expansion of the Clinical SpectrumMonique E De Paepe, Lawrence Young, Julie R Jones, et al.
Genesis (New York, N.Y. : 2000)|August 3, 2004
Efficient DNA cassette exchange in mouse embryonic stem cells by staggered positive-negative selectionQiaoming Long, Kathy D Shelton, Jill Lindner, et al.
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
Current Protocols in Human Genetics|February 11, 2014
Nonrandom X chromosome inactivation detectionJulie R Jones
American Journal of Medical Genetics. Part A|April 7, 2020
Fatal hyperkeratosis syndrome in four siblings due to dolichol kinase deficiencyBryan D Hall, Roger E Stevenson, Julie R Jones
Multiple Sclerosis and Related Disorders|May 12, 2018
Forkhead box C1 gene variant causing glaucoma and small vessel angiopathy can mimic multiple sclerosisJagannadha R Avasarala, Julie R Jones, Curtis R Rogers
Nutrition Reviews|February 24, 2006
Dietary reference intakes: implications for fiber labeling and consumption: a summary of the International Life Sciences Institute North America Fiber Workshop, June 1-2, 2004, Washington, DCJulie R Jones, David M Lineback, Marci J Levine
Methods in Molecular Medicine|November 16, 2004
Strategies for the use of site-specific recombinases in genome engineeringJulie R Jones, Kathy D Shelton, Mark A Magnuson
Journal of Inherited Metabolic Disease|September 15, 2012
Molecular characterization of 355 mucopolysaccharidosis patients reveals 104 novel mutationsLaura M Pollard, Julie R Jones, Tim C Wood
European Journal of Medical Genetics|February 28, 2016
CHD8 intragenic deletion associated with autism spectrum disorderElliot S Stolerman, Brooke Smith, Alka Chaubey, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Classic phenotype of Coffin-Lowry syndrome in a female with stimulus-induced drop episodes and a genotype with preserved N-terminal kinase domainKitiwan Rojnueangnit, Julie R Jones, Monica J Basehore, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 14, 2018
Ovotesticular Disorder of Sex Development (Ovotestis) in Simpson-Golabi-Behmel Syndrome: Expansion of the Clinical SpectrumMonique E De Paepe, Lawrence Young, Julie R Jones, et al.
Genesis (New York, N.Y. : 2000)|August 3, 2004
Efficient DNA cassette exchange in mouse embryonic stem cells by staggered positive-negative selectionQiaoming Long, Kathy D Shelton, Jill Lindner, et al.
Pageof 7