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

L A Larsen

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
European Journal of Medical Genetics|November 14, 2007
Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephalyF Erdogan, J M Belloso, E Gabau, et al.
Clinical Chemistry|July 27, 2001
Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndromeL A Larsen, P S Andersen, J Kanters, et al.
Scandinavian Journal of Immunology|June 11, 2009
Genome-wide gene expression profiling of SCID mice with T-cell-mediated ColitisD Brudzewsky, A E Pedersen, M H Claesson, et al.
Journal of Medical Genetics|August 21, 2008
High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart diseaseF Erdogan, L A Larsen, L Zhang, et al.
Clinical Genetics|March 29, 2000
Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2L A Larsen, I H Svendsen, A M Jensen, et al.
Journal of Medical Genetics|July 17, 2008
Mapping of 5q35 chromosomal rearrangements within a genomically unstable regionK Buysse, A Crepel, B Menten, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
Scientific Reports|June 24, 2018
The E3 ubiquitin ligase SMURF1 regulates cell-fate specification and outflow tract septation during mammalian heart developmentK Koefoed, J Skat-Rørdam, P Andersen, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
European Journal of Medical Genetics|November 14, 2007
Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephalyF Erdogan, J M Belloso, E Gabau, et al.
Clinical Chemistry|July 27, 2001
Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndromeL A Larsen, P S Andersen, J Kanters, et al.
Scandinavian Journal of Immunology|June 11, 2009
Genome-wide gene expression profiling of SCID mice with T-cell-mediated ColitisD Brudzewsky, A E Pedersen, M H Claesson, et al.
Journal of Medical Genetics|August 21, 2008
High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart diseaseF Erdogan, L A Larsen, L Zhang, et al.
Clinical Genetics|March 29, 2000
Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2L A Larsen, I H Svendsen, A M Jensen, et al.
Journal of Medical Genetics|July 17, 2008
Mapping of 5q35 chromosomal rearrangements within a genomically unstable regionK Buysse, A Crepel, B Menten, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
Scientific Reports|June 24, 2018
The E3 ubiquitin ligase SMURF1 regulates cell-fate specification and outflow tract septation during mammalian heart developmentK Koefoed, J Skat-Rørdam, P Andersen, et al.
Pageof 4