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

C Boileau

Showing results (91-100 of 127) with videos related to

Pageof 13
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 22, 2008
A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic familyA Jelassi, M Najah, I Jguirim, et al.
Atherosclerosis|September 2, 2008
Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in TunisiaA Jelassi, I Jguirim, M Najah, et al.
Scandinavian Journal of Rheumatology|March 24, 2009
Association of hypoxia-inducible factor 1A (HIF1A) gene polymorphisms with systemic sclerosis in a French European Caucasian populationJ Wipff, P Dieude, J Avouac, et al.
American Journal of Medical Genetics. Part A|November 25, 2024
De Novo Balanced Translocations Disrupting the FBN1 Gene Diagnosed by Genome Sequencing: An Uncommon Cause of Marfan Syndrome Modifying Genetic CounselingC Racine, P Callier, R Touraine, et al.
Arthritis and Rheumatism|June 26, 2008
The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysisP Dieudé, M Guedj, J Wipff, et al.
Journal of Medical Genetics|January 15, 2003
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndromeL Faivre, R J Gorlin, M K Wirtz, et al.
Journal of Medical Genetics|August 19, 2008
A PCSK9 variant and familial combined hyperlipidaemiaM Abifadel, L Bernier, G Dubuc, et al.
European Heart Journal|August 21, 2001
Diagnosis and management of aortic dissectionR Erbel, F Alfonso, C Boileau, et al.
Nucleic Acids Research|January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneG Collod-Béroud, C Béroud, L Adès, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defectsB Saint-Jore, M Varret, C Dachet, et al.
Pageof 13

Showing results (91-100 of 127) with videos related to

Sort By:
Pageof 13
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 22, 2008
A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic familyA Jelassi, M Najah, I Jguirim, et al.
Atherosclerosis|September 2, 2008
Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in TunisiaA Jelassi, I Jguirim, M Najah, et al.
Scandinavian Journal of Rheumatology|March 24, 2009
Association of hypoxia-inducible factor 1A (HIF1A) gene polymorphisms with systemic sclerosis in a French European Caucasian populationJ Wipff, P Dieude, J Avouac, et al.
American Journal of Medical Genetics. Part A|November 25, 2024
De Novo Balanced Translocations Disrupting the FBN1 Gene Diagnosed by Genome Sequencing: An Uncommon Cause of Marfan Syndrome Modifying Genetic CounselingC Racine, P Callier, R Touraine, et al.
Arthritis and Rheumatism|June 26, 2008
The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysisP Dieudé, M Guedj, J Wipff, et al.
Journal of Medical Genetics|January 15, 2003
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndromeL Faivre, R J Gorlin, M K Wirtz, et al.
Journal of Medical Genetics|August 19, 2008
A PCSK9 variant and familial combined hyperlipidaemiaM Abifadel, L Bernier, G Dubuc, et al.
European Heart Journal|August 21, 2001
Diagnosis and management of aortic dissectionR Erbel, F Alfonso, C Boileau, et al.
Nucleic Acids Research|January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneG Collod-Béroud, C Béroud, L Adès, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defectsB Saint-Jore, M Varret, C Dachet, et al.
Pageof 13