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

A DE Paepe

Showing results (61-70 of 173) with videos related to

Pageof 18
Sort By:
Bone|December 13, 2002
Vitamin D receptor gene allelic variants, bone density, and bone turnover in community-dwelling menI Van Pottelbergh, S Goemaere, D De Bacquer, et al.
VASA. Zeitschrift Fur Gefasskrankheiten|September 19, 2002
Acute intramural haematoma of the coeliac arteryH J Kruse, M Weise, L Nuytinck, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 22, 2001
Association of the type I collagen alpha1 Sp1 polymorphism, bone density and upper limb muscle strength in community-dwelling elderly menI Van Pottelbergh, S Goemaere, L Nuytinck, et al.
Journal of Medical Genetics|July 4, 2006
Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problemsF Malfait, S Symoens, P Coucke, et al.
Disease Markers|December 14, 1999
Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > GK Claes, E Machackova, M De Vos, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology|July 5, 2005
The use of Tissue Doppler Imaging for the assessment of changes in myocardial structure and function in inherited cardiomyopathiesJ De Backer, D Matthys, T C Gillebert, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Osteogenesis imperfecta phenotypes resulting from serine for glycine substitutions in the alpha2(I) collagen chainL Nuytinck, K Wettinck, M Freund, et al.
Clinical Genetics|August 28, 2007
Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndromeJ De Backer, B Loeys, B Leroy, et al.
Human Reproduction (Oxford, England)|April 1, 1997
Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryosH Laverge, P De Sutter, M R Verschraegen-Spae, et al.
Human Mutation|March 25, 1999
Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. OnlineK Claes, E Machackova, M De Vos, et al.
Pageof 18

Showing results (61-70 of 173) with videos related to

Sort By:
Pageof 18
Bone|December 13, 2002
Vitamin D receptor gene allelic variants, bone density, and bone turnover in community-dwelling menI Van Pottelbergh, S Goemaere, D De Bacquer, et al.
VASA. Zeitschrift Fur Gefasskrankheiten|September 19, 2002
Acute intramural haematoma of the coeliac arteryH J Kruse, M Weise, L Nuytinck, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 22, 2001
Association of the type I collagen alpha1 Sp1 polymorphism, bone density and upper limb muscle strength in community-dwelling elderly menI Van Pottelbergh, S Goemaere, L Nuytinck, et al.
Journal of Medical Genetics|July 4, 2006
Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problemsF Malfait, S Symoens, P Coucke, et al.
Disease Markers|December 14, 1999
Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > GK Claes, E Machackova, M De Vos, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology|July 5, 2005
The use of Tissue Doppler Imaging for the assessment of changes in myocardial structure and function in inherited cardiomyopathiesJ De Backer, D Matthys, T C Gillebert, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Osteogenesis imperfecta phenotypes resulting from serine for glycine substitutions in the alpha2(I) collagen chainL Nuytinck, K Wettinck, M Freund, et al.
Clinical Genetics|August 28, 2007
Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndromeJ De Backer, B Loeys, B Leroy, et al.
Human Reproduction (Oxford, England)|April 1, 1997
Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryosH Laverge, P De Sutter, M R Verschraegen-Spae, et al.
Human Mutation|March 25, 1999
Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. OnlineK Claes, E Machackova, M De Vos, et al.
Pageof 18