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

B Assouline

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2010
[Autism announcement at consultation is a therapeutic step]B Assouline
L'Encephale|September 12, 2015
[Schooling of patients exhibiting Autism Spectrum Disorders without mental retardation]D Grimm, B Assouline, A Piero
Experimental Parasitology|April 1, 1996
Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genesS Bretagne, B Assouline, D Vidaud, et al.
Annales De Genetique|January 1, 1997
Myotonic dystrophy protein kinase gene expression in skeletal muscle from congenitally affected infantsA Laurent, J M Costa, B Assouline, et al.
Neurology|May 1, 1996
Misdiagnosis revealed by genetic linkage analysis in a family with Wilson diseaseD Vidaud, B Assouline, P Lecoz, et al.
Journal of Clinical Microbiology|October 8, 1997
Microsatellite in the beta-tubulin gene of Toxoplasma gondii as a new genetic marker for use in direct screening of amniotic fluidsJ M Costa, M L Dardé, B Assouline, et al.
Infection and Immunity|October 21, 2015
Treatment with Interleukin-7 Restores Host Defense against Pneumocystis in CD4+ T-Lymphocyte-Depleted MiceS Ruan, D R Samuelson, B Assouline, et al.
Journal of Molecular Biology|April 9, 2001
A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definitionL J Fang, M J Simard, D Vidaud, et al.
Journal of Intellectual Disability Research : JIDR|July 17, 2008
What clinical characteristics of children with autism influence their inclusion in regular classrooms?C Yianni-Coudurier, C Darrou, P Lenoir, et al.
American Journal of Medical Genetics|February 25, 1998
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndromeM Bahuau, C Houdayer, B Assouline, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2010
[Autism announcement at consultation is a therapeutic step]B Assouline
L'Encephale|September 12, 2015
[Schooling of patients exhibiting Autism Spectrum Disorders without mental retardation]D Grimm, B Assouline, A Piero
Experimental Parasitology|April 1, 1996
Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genesS Bretagne, B Assouline, D Vidaud, et al.
Annales De Genetique|January 1, 1997
Myotonic dystrophy protein kinase gene expression in skeletal muscle from congenitally affected infantsA Laurent, J M Costa, B Assouline, et al.
Neurology|May 1, 1996
Misdiagnosis revealed by genetic linkage analysis in a family with Wilson diseaseD Vidaud, B Assouline, P Lecoz, et al.
Journal of Clinical Microbiology|October 8, 1997
Microsatellite in the beta-tubulin gene of Toxoplasma gondii as a new genetic marker for use in direct screening of amniotic fluidsJ M Costa, M L Dardé, B Assouline, et al.
Infection and Immunity|October 21, 2015
Treatment with Interleukin-7 Restores Host Defense against Pneumocystis in CD4+ T-Lymphocyte-Depleted MiceS Ruan, D R Samuelson, B Assouline, et al.
Journal of Molecular Biology|April 9, 2001
A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definitionL J Fang, M J Simard, D Vidaud, et al.
Journal of Intellectual Disability Research : JIDR|July 17, 2008
What clinical characteristics of children with autism influence their inclusion in regular classrooms?C Yianni-Coudurier, C Darrou, P Lenoir, et al.
American Journal of Medical Genetics|February 25, 1998
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndromeM Bahuau, C Houdayer, B Assouline, et al.
Pageof 2