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

Anne De Paepe

Showing results (61-70 of 236) with videos related to

Pageof 24
Sort By:
Arthritis Care & Research|July 28, 2011
Balance, gait, falls, and fear of falling in women with the hypermobility type of Ehlers-Danlos syndromeLies Rombaut, Fransiska Malfait, Inge De Wandele, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2014
Loeys-Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signalingReed Pyeritz, Guillaume Jondeau, Rocio Moran, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrumAlexander Janssen, Mohammad J Hosen, Philippe Jeannin, et al.
Acta Cardiologica|June 29, 2017
Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trialLaura Muiño-Mosquera, Sylvia De Nobele, Daniel Devos, et al.
American Journal of Human Genetics|March 13, 2003
Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hipsJan Hellemans, Paul J Coucke, Andres Giedion, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
A genome-wide linkage scan for low spinal bone mineral density in a single extended family confirms linkage to 1p36.3Andy Willaert, Inge Van Pottelbergh, Hans Zmierczak, et al.
Personalized Medicine|May 15, 2018
Attitudes of cystic fibrosis patients and their parents towards direct-to-consumer genetic testing for carrier statusSandra Janssens, Louiza Kalokairinou, Davit Chokoshvilli, et al.
European Journal of Human Genetics : EJHG|April 28, 2011
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypesMine Arslan-Kirchner, Jörg T Epplen, Laurence Faivre, et al.
Human Molecular Genetics|March 29, 2008
Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivationDiane Beysen, Lara Moumné, Reiner Veitia, et al.
Disease Models & Mechanisms|October 26, 2018
CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragmentsAnnekatrien Boel, Hanna De Saffel, Wouter Steyaert, et al.
Pageof 24

Showing results (61-70 of 236) with videos related to

Sort By:
Pageof 24
Arthritis Care & Research|July 28, 2011
Balance, gait, falls, and fear of falling in women with the hypermobility type of Ehlers-Danlos syndromeLies Rombaut, Fransiska Malfait, Inge De Wandele, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2014
Loeys-Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signalingReed Pyeritz, Guillaume Jondeau, Rocio Moran, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrumAlexander Janssen, Mohammad J Hosen, Philippe Jeannin, et al.
Acta Cardiologica|June 29, 2017
Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trialLaura Muiño-Mosquera, Sylvia De Nobele, Daniel Devos, et al.
American Journal of Human Genetics|March 13, 2003
Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hipsJan Hellemans, Paul J Coucke, Andres Giedion, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
A genome-wide linkage scan for low spinal bone mineral density in a single extended family confirms linkage to 1p36.3Andy Willaert, Inge Van Pottelbergh, Hans Zmierczak, et al.
Personalized Medicine|May 15, 2018
Attitudes of cystic fibrosis patients and their parents towards direct-to-consumer genetic testing for carrier statusSandra Janssens, Louiza Kalokairinou, Davit Chokoshvilli, et al.
European Journal of Human Genetics : EJHG|April 28, 2011
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypesMine Arslan-Kirchner, Jörg T Epplen, Laurence Faivre, et al.
Human Molecular Genetics|March 29, 2008
Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivationDiane Beysen, Lara Moumné, Reiner Veitia, et al.
Disease Models & Mechanisms|October 26, 2018
CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragmentsAnnekatrien Boel, Hanna De Saffel, Wouter Steyaert, et al.
Pageof 24