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Cathrine Jespersgaard

Showing results (31-40 of 37) with videos related to

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Scientific Reports|February 6, 2019
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophyCathrine Jespersgaard, Mingyan Fang, Mette Bertelsen, et al.
Investigative Ophthalmology & Visual Science|February 22, 2020
A Missense Mutation in RAB28 in a Family with Cone-Rod Dystrophy and Postaxial Polydactyly Prevents Localization of RAB28 to the Primary CiliumCathrine Jespersgaard, Amalie Brunbjerg Hey, Tomas Ilginis, et al.
Journal of Crohn'S & Colitis|December 22, 2010
Genetic and environmental factors as predictors of disease severity and extent at time of diagnosis in an inception cohort of inflammatory bowel disease, Copenhagen County and City 2003-2005Ida Vind, Lene Riis, Cathrine Jespersgaard, et al.
Clinical Genetics|November 13, 2018
Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movementsBitten Schönewolf-Greulich, Anne-Marie Bisgaard, Morten Dunø, et al.
Plos Genetics|November 13, 2018
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterizationLusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, et al.
Frontiers in Neuroscience|September 8, 2016
TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette SyndromeNatalie J Forde, Ahmad S Kanaan, Joanna Widomska, et al.
American Journal of Medical Genetics. Part A|May 27, 2017
Phenotypes and genotypes in individuals with SMC1A variantsSylvia Huisman, Paul A Mulder, Egbert Redeker, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Scientific Reports|February 6, 2019
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophyCathrine Jespersgaard, Mingyan Fang, Mette Bertelsen, et al.
Investigative Ophthalmology & Visual Science|February 22, 2020
A Missense Mutation in RAB28 in a Family with Cone-Rod Dystrophy and Postaxial Polydactyly Prevents Localization of RAB28 to the Primary CiliumCathrine Jespersgaard, Amalie Brunbjerg Hey, Tomas Ilginis, et al.
Journal of Crohn'S & Colitis|December 22, 2010
Genetic and environmental factors as predictors of disease severity and extent at time of diagnosis in an inception cohort of inflammatory bowel disease, Copenhagen County and City 2003-2005Ida Vind, Lene Riis, Cathrine Jespersgaard, et al.
Clinical Genetics|November 13, 2018
Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movementsBitten Schönewolf-Greulich, Anne-Marie Bisgaard, Morten Dunø, et al.
Plos Genetics|November 13, 2018
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterizationLusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, et al.
Frontiers in Neuroscience|September 8, 2016
TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette SyndromeNatalie J Forde, Ahmad S Kanaan, Joanna Widomska, et al.
American Journal of Medical Genetics. Part A|May 27, 2017
Phenotypes and genotypes in individuals with SMC1A variantsSylvia Huisman, Paul A Mulder, Egbert Redeker, et al.
Pageof 4