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

Gilgenkrantz

Showing results (81-90 of 233) with videos related to

Pageof 24
Sort By:
Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.
Nature|October 13, 1983
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour associationC Huerre, S Despoisse, S Gilgenkrantz, et al.
Human Genetics|February 1, 1996
X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probeP Camus, N Abbadi, M C Perrier, et al.
Pediatrie|January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]C Pernot, A M Worms, F Marçon, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Molecular pathology of Duchenne and Becker muscular dystrophy]H Gilgenkrantz, J Chelly, D Récan, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|November 1, 1992
[Rehabilitation centers: for whom? Why and how long?]P C Goepfert, J J Maureira, T Courtalon, et al.
Journal De Genetique Humaine|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Illegitimate transcription: discovery and application to gene molecular pathology]J C Kaplan, J Chelly, H Gilgenkrantz, et al.
Journal De Genetique Humaine|July 1, 1984
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]S Gilgenkrantz, M J Gregoire, M Chery, et al.
American Journal of Medical Genetics|September 1, 1982
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathyS Gilgenkrantz, C Vigneron, M J Gregoire, et al.
Pageof 24

Showing results (81-90 of 233) with videos related to

Sort By:
Pageof 24
Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.
Nature|October 13, 1983
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour associationC Huerre, S Despoisse, S Gilgenkrantz, et al.
Human Genetics|February 1, 1996
X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probeP Camus, N Abbadi, M C Perrier, et al.
Pediatrie|January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]C Pernot, A M Worms, F Marçon, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Molecular pathology of Duchenne and Becker muscular dystrophy]H Gilgenkrantz, J Chelly, D Récan, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|November 1, 1992
[Rehabilitation centers: for whom? Why and how long?]P C Goepfert, J J Maureira, T Courtalon, et al.
Journal De Genetique Humaine|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Illegitimate transcription: discovery and application to gene molecular pathology]J C Kaplan, J Chelly, H Gilgenkrantz, et al.
Journal De Genetique Humaine|July 1, 1984
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]S Gilgenkrantz, M J Gregoire, M Chery, et al.
American Journal of Medical Genetics|September 1, 1982
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathyS Gilgenkrantz, C Vigneron, M J Gregoire, et al.
Pageof 24