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

M M Mannens

Showing results (11-20 of 22) with videos related to

Pageof 3
Sort By:
Cytogenetics and Cell Genetics|June 1, 2000
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumorsM J Steenman, N Zijlstra, D L Kruitbosch, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23A Bout, J M Hoovers, E Bakker, et al.
The Journal of Biological Chemistry|September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiencyR G Boot, G H Renkema, M Verhoek, et al.
Clinical Genetics|March 29, 2000
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The NetherlandsM P Lombardi, E J Redeker, J C Defesche, et al.
Nature Genetics|September 2, 1999
Cardiac conduction defects associate with mutations in SCN5AJ J Schott, C Alshinawi, F Kyndt, et al.
Cardiovascular Research|February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndromeM B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Human Mutation|January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic valueR G Boot, C E Hollak, M Verhoek, et al.
Human Mutation|April 8, 2011
Mutation update for the PORCN geneMaria Paola Lombardi, Saskia Bulk, Jacopo Celli, et al.
Atherosclerosis|October 10, 2008
Low HDL cholesterol levels in type I Gaucher disease do not lead to an increased risk of cardiovascular diseaseM de Fost, M Langeveld, R Franssen, et al.
Atherosclerosis|May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosisA A W Weterings, I A W van Rijsingen, A S Plomp, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Cytogenetics and Cell Genetics|June 1, 2000
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumorsM J Steenman, N Zijlstra, D L Kruitbosch, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23A Bout, J M Hoovers, E Bakker, et al.
The Journal of Biological Chemistry|September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiencyR G Boot, G H Renkema, M Verhoek, et al.
Clinical Genetics|March 29, 2000
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The NetherlandsM P Lombardi, E J Redeker, J C Defesche, et al.
Nature Genetics|September 2, 1999
Cardiac conduction defects associate with mutations in SCN5AJ J Schott, C Alshinawi, F Kyndt, et al.
Cardiovascular Research|February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndromeM B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Human Mutation|January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic valueR G Boot, C E Hollak, M Verhoek, et al.
Human Mutation|April 8, 2011
Mutation update for the PORCN geneMaria Paola Lombardi, Saskia Bulk, Jacopo Celli, et al.
Atherosclerosis|October 10, 2008
Low HDL cholesterol levels in type I Gaucher disease do not lead to an increased risk of cardiovascular diseaseM de Fost, M Langeveld, R Franssen, et al.
Atherosclerosis|May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosisA A W Weterings, I A W van Rijsingen, A S Plomp, et al.
Pageof 3