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 Mimault

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Human Genetics|August 1, 1995
Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneC Mimault, F Cailloux, G Giraud, et al.
American Journal of Human Genetics|July 27, 1999
Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating DiseaseC Mimault, G Giraud, V Courtois, et al.
American Journal of Human Genetics|September 1, 1994
Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical GroupO Boespflug-Tanguy, C Mimault, J Melki, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating DiseaseF Cailloux, F Gauthier-Barichard, C Mimault, et al.
Human Molecular Genetics|April 1, 1993
Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid geneD Pham-Dinh, O Boespflug-Tanguy, C Mimault, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Human Genetics|August 1, 1995
Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneC Mimault, F Cailloux, G Giraud, et al.
American Journal of Human Genetics|July 27, 1999
Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating DiseaseC Mimault, G Giraud, V Courtois, et al.
American Journal of Human Genetics|September 1, 1994
Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical GroupO Boespflug-Tanguy, C Mimault, J Melki, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating DiseaseF Cailloux, F Gauthier-Barichard, C Mimault, et al.
Human Molecular Genetics|April 1, 1993
Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid geneD Pham-Dinh, O Boespflug-Tanguy, C Mimault, et al.
Pageof 1