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 Bonithon-Kopp

Showing results (61-70 of 71) with videos related to

Pageof 8
Sort By:
British Journal of Cancer|August 15, 2002
Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomasC Chapusot, L Martin, A M Bouvier, et al.
European Journal of Medical Genetics|March 23, 2011
Written information to patients in clinical genetics: what's the impact?C Cassini, C Thauvin-Robinet, S Vinault, et al.
Journal of Thrombosis and Haemostasis : JTH|April 1, 2014
Annual diagnosis rate of superficial vein thrombosis of the lower limbs: the STEPH community-based studyP Frappé, A Buchmuller-Cordier, L Bertoletti, et al.
Alimentary Pharmacology & Therapeutics|April 9, 2005
Is the management of hepatitis C patients appropriate? A population-based studyC Hatem, A Minello, S Bresson-Hadni, et al.
European Journal of Endocrinology|May 10, 2011
Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs EndocrinesP Goudet, C Bonithon-Kopp, A Murat, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterionL Faivre, G Collod-Beroud, B Callewaert, et al.
Journal of Medical Genetics|March 4, 2008
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probandsL Faivre, G Collod-Beroud, A Child, et al.
European Journal of Human Genetics : EJHG|November 13, 2008
Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutationL Faivre, G Collod-Beroud, B Callewaert, et al.
Clinical Genetics|May 14, 2011
The new Ghent criteria for Marfan syndrome: what do they change?L Faivre, G Collod-Beroud, L Adès, et al.
American Journal of Human Genetics|August 19, 2007
Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international studyL Faivre, G Collod-Beroud, B L Loeys, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
British Journal of Cancer|August 15, 2002
Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomasC Chapusot, L Martin, A M Bouvier, et al.
European Journal of Medical Genetics|March 23, 2011
Written information to patients in clinical genetics: what's the impact?C Cassini, C Thauvin-Robinet, S Vinault, et al.
Journal of Thrombosis and Haemostasis : JTH|April 1, 2014
Annual diagnosis rate of superficial vein thrombosis of the lower limbs: the STEPH community-based studyP Frappé, A Buchmuller-Cordier, L Bertoletti, et al.
Alimentary Pharmacology & Therapeutics|April 9, 2005
Is the management of hepatitis C patients appropriate? A population-based studyC Hatem, A Minello, S Bresson-Hadni, et al.
European Journal of Endocrinology|May 10, 2011
Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs EndocrinesP Goudet, C Bonithon-Kopp, A Murat, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterionL Faivre, G Collod-Beroud, B Callewaert, et al.
Journal of Medical Genetics|March 4, 2008
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probandsL Faivre, G Collod-Beroud, A Child, et al.
European Journal of Human Genetics : EJHG|November 13, 2008
Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutationL Faivre, G Collod-Beroud, B Callewaert, et al.
Clinical Genetics|May 14, 2011
The new Ghent criteria for Marfan syndrome: what do they change?L Faivre, G Collod-Beroud, L Adès, et al.
American Journal of Human Genetics|August 19, 2007
Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international studyL Faivre, G Collod-Beroud, B L Loeys, et al.
Pageof 8