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 Kleta

Showing results (21-30 of 166) with videos related to

Pageof 17
Sort By:
Rare Diseases (Austin, Tex.)|August 9, 2016
EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10Ola Abdelhadi, Daniela Iancu, Horia Stanescu, et al.
Journal of Child Neurology|January 19, 2006
Novel form of intermediate salla disease: clinical and neuroimaging featuresRichard P Morse, Robert Kleta, Joseph Alroy, et al.
Bioinformatics (Oxford, England)|December 15, 2012
SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPUAlan Medlar, Dorota Głowacka, Horia Stanescu, et al.
Bioinformatics (Oxford, England)|September 30, 2017
HaploForge: a comprehensive pedigree drawing and haplotype visualization web applicationMehmet Tekman, Alan Medlar, Monika Mozere, et al.
Molecular Genetics and Metabolism|April 28, 2004
Renal glucosuria due to SGLT2 mutationsRobert Kleta, Caroline Stuart, Fred A Gill, et al.
Pediatric Nephrology (Berlin, Germany)|May 28, 2011
Genetic testing in renal diseaseDetlef Bockenhauer, Alan J Medlar, Emma Ashton, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 3, 2020
Inherited Tubulopathies of the Kidney: Insights from GeneticsMallory L Downie, Sergio C Lopez Garcia, Robert Kleta, et al.
Medicine|May 10, 2005
Swallowing dysfunction in 101 patients with nephropathic cystinosis: benefit of long-term cysteamine therapyBarbara C Sonies, Phaedra Almajid, Robert Kleta, et al.
Pediatric Nephrology (Berlin, Germany)|October 21, 2020
Novel insights in the genetics of steroid-sensitive nephrotic syndrome in childhoodStephanie Dufek-Kamperis, Robert Kleta, Detlef Bockenhauer, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika Mozere, Mehmet Tekman, Jameela Kari, et al.
Pageof 17

Showing results (21-30 of 166) with videos related to

Sort By:
Pageof 17
Rare Diseases (Austin, Tex.)|August 9, 2016
EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10Ola Abdelhadi, Daniela Iancu, Horia Stanescu, et al.
Journal of Child Neurology|January 19, 2006
Novel form of intermediate salla disease: clinical and neuroimaging featuresRichard P Morse, Robert Kleta, Joseph Alroy, et al.
Bioinformatics (Oxford, England)|December 15, 2012
SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPUAlan Medlar, Dorota Głowacka, Horia Stanescu, et al.
Bioinformatics (Oxford, England)|September 30, 2017
HaploForge: a comprehensive pedigree drawing and haplotype visualization web applicationMehmet Tekman, Alan Medlar, Monika Mozere, et al.
Molecular Genetics and Metabolism|April 28, 2004
Renal glucosuria due to SGLT2 mutationsRobert Kleta, Caroline Stuart, Fred A Gill, et al.
Pediatric Nephrology (Berlin, Germany)|May 28, 2011
Genetic testing in renal diseaseDetlef Bockenhauer, Alan J Medlar, Emma Ashton, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 3, 2020
Inherited Tubulopathies of the Kidney: Insights from GeneticsMallory L Downie, Sergio C Lopez Garcia, Robert Kleta, et al.
Medicine|May 10, 2005
Swallowing dysfunction in 101 patients with nephropathic cystinosis: benefit of long-term cysteamine therapyBarbara C Sonies, Phaedra Almajid, Robert Kleta, et al.
Pediatric Nephrology (Berlin, Germany)|October 21, 2020
Novel insights in the genetics of steroid-sensitive nephrotic syndrome in childhoodStephanie Dufek-Kamperis, Robert Kleta, Detlef Bockenhauer, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika Mozere, Mehmet Tekman, Jameela Kari, et al.
Pageof 17