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

J FREZAL

Showing results (41-50 of 61) with videos related to

Pageof 7
Sort By:
Annales De Medecine Interne|January 1, 1982
[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum]H Ogier, J M Saudubray, C Charpentier, et al.
Human Genetics|April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's diseaseS Gerber, J M Rozet, D Bonneau, et al.
Annales De Biologie Clinique|January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]A Pelet, E Toumas, D Rabier, et al.
Archives Francaises De Pediatrie|December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]F X Coude, H Ogier, C Charpentier, et al.
Lancet (London, England)|August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy InvestigatorsJ Melki, P Sheth, S Abdelhak, et al.
Human Genetics|January 1, 1980
Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16V C Nguyen, D Weil, M C Hors-Cayla, et al.
Lancet (London, England)|September 3, 1988
Deletion of blood mitochondrial DNA in pancytopeniaA Rötig, M Colonna, S Blanche, et al.
Journal of Medical Genetics|March 1, 1994
Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinosesS Gerber, S Odent, A Postel-Vinay, et al.
Journal De Genetique Humaine|November 1, 1976
[The genetics of congenital glaucoma: a study of 231 cases]M L Briard, J Feingold, J Kaplan, et al.
Human Genetics|January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorderF X Coude, H Ogier, C Charpentier, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Annales De Medecine Interne|January 1, 1982
[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum]H Ogier, J M Saudubray, C Charpentier, et al.
Human Genetics|April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's diseaseS Gerber, J M Rozet, D Bonneau, et al.
Annales De Biologie Clinique|January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]A Pelet, E Toumas, D Rabier, et al.
Archives Francaises De Pediatrie|December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]F X Coude, H Ogier, C Charpentier, et al.
Lancet (London, England)|August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy InvestigatorsJ Melki, P Sheth, S Abdelhak, et al.
Human Genetics|January 1, 1980
Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16V C Nguyen, D Weil, M C Hors-Cayla, et al.
Lancet (London, England)|September 3, 1988
Deletion of blood mitochondrial DNA in pancytopeniaA Rötig, M Colonna, S Blanche, et al.
Journal of Medical Genetics|March 1, 1994
Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinosesS Gerber, S Odent, A Postel-Vinay, et al.
Journal De Genetique Humaine|November 1, 1976
[The genetics of congenital glaucoma: a study of 231 cases]M L Briard, J Feingold, J Kaplan, et al.
Human Genetics|January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorderF X Coude, H Ogier, C Charpentier, et al.
Pageof 7