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

Bertrand Chevallier

Showing results (31-40 of 37) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 37 results.
European Journal of Human Genetics : EJHG|March 19, 2009
Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 geneChantal Stheneur, Gwenaëlle Collod-Béroud, Laurence Faivre, et al.
Archives of Cardiovascular Diseases|November 19, 2019
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndromeSebastien Hascoet, Thomas Edouard, Julie Plaisancie, et al.
Pediatric Research|December 8, 2010
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 yearChantal Stheneur, Laurence Faivre, Gwenaëlle Collod-Béroud, et al.
Human Mutation|September 11, 2008
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disordersChantal Stheneur, Gwenaëlle Collod-Béroud, Laurence Faivre, et al.
The Lancet. Digital Health|December 16, 2020
A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth chartsBarbara Heude, Pauline Scherdel, Andreas Werner, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 29, 2006
[Recommendations for the medical management of aortic complications of Marfan's syndrome]Guillaume Jondeau, Martine Barthelet, Clarisse Baumann, et al.
Pediatrics|January 2, 2009
Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutationsLaurence Faivre, Alice Masurel-Paulet, Gwenaëlle Collod-Béroud, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
European Journal of Human Genetics : EJHG|March 19, 2009
Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 geneChantal Stheneur, Gwenaëlle Collod-Béroud, Laurence Faivre, et al.
Archives of Cardiovascular Diseases|November 19, 2019
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndromeSebastien Hascoet, Thomas Edouard, Julie Plaisancie, et al.
Pediatric Research|December 8, 2010
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 yearChantal Stheneur, Laurence Faivre, Gwenaëlle Collod-Béroud, et al.
Human Mutation|September 11, 2008
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disordersChantal Stheneur, Gwenaëlle Collod-Béroud, Laurence Faivre, et al.
The Lancet. Digital Health|December 16, 2020
A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth chartsBarbara Heude, Pauline Scherdel, Andreas Werner, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 29, 2006
[Recommendations for the medical management of aortic complications of Marfan's syndrome]Guillaume Jondeau, Martine Barthelet, Clarisse Baumann, et al.
Pediatrics|January 2, 2009
Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutationsLaurence Faivre, Alice Masurel-Paulet, Gwenaëlle Collod-Béroud, et al.
Pageof 4