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 Besmond

Showing results (11-20 of 41) with videos related to

Pageof 5
Sort By:
Human Molecular Genetics|July 1, 1993
Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencingV Blanquet, C Turleau, M S Gross, et al.
Annales De Medecine Interne|January 1, 1985
[Study of hereditary fructose intolerance by methods of molecular biology]J C Dreyfus, F Schapira, C Besmond, et al.
Annals of Human Genetics|October 1, 1984
DNA analysis in patients with hereditary fructose intoleranceC Grégori, C Besmond, M Odievre, et al.
Human Mutation|January 1, 1993
Detection of sequence variations in the human insulin-receptor gene by parallel denaturing gradient gel electrophoresisC Desbois, J Magré, V Blanquet, et al.
Journal of Medical Genetics|May 23, 2001
The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosisM Gabolde, D Hubert, M Guilloud-Bataille, et al.
Pediatric Research|May 1, 1982
Cell-free translation of messenger RNAs from human muscle biopsies: a miniaturized tool for investigation of neuromuscular diseasesA Munnich, D Daegelen, C Besmond, et al.
Human Molecular Genetics|July 1, 1994
Three novel germline mutations in exons 8 and 18 of the retinoblastoma geneV Blanquet, M S Gross, C Turleau, et al.
The Journal of Clinical Investigation|March 1, 1985
Dietary and hormonal regulation of aldolase B gene expressionA Munnich, C Besmond, S Darquy, et al.
Genomics|July 1, 1992
Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctionsP Fanen, N Ghanem, M Vidaud, et al.
Human Molecular Genetics|March 1, 1995
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastomaV Blanquet, C Turleau, M S Gross-Morand, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|July 1, 1993
Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencingV Blanquet, C Turleau, M S Gross, et al.
Annales De Medecine Interne|January 1, 1985
[Study of hereditary fructose intolerance by methods of molecular biology]J C Dreyfus, F Schapira, C Besmond, et al.
Annals of Human Genetics|October 1, 1984
DNA analysis in patients with hereditary fructose intoleranceC Grégori, C Besmond, M Odievre, et al.
Human Mutation|January 1, 1993
Detection of sequence variations in the human insulin-receptor gene by parallel denaturing gradient gel electrophoresisC Desbois, J Magré, V Blanquet, et al.
Journal of Medical Genetics|May 23, 2001
The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosisM Gabolde, D Hubert, M Guilloud-Bataille, et al.
Pediatric Research|May 1, 1982
Cell-free translation of messenger RNAs from human muscle biopsies: a miniaturized tool for investigation of neuromuscular diseasesA Munnich, D Daegelen, C Besmond, et al.
Human Molecular Genetics|July 1, 1994
Three novel germline mutations in exons 8 and 18 of the retinoblastoma geneV Blanquet, M S Gross, C Turleau, et al.
The Journal of Clinical Investigation|March 1, 1985
Dietary and hormonal regulation of aldolase B gene expressionA Munnich, C Besmond, S Darquy, et al.
Genomics|July 1, 1992
Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctionsP Fanen, N Ghanem, M Vidaud, et al.
Human Molecular Genetics|March 1, 1995
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastomaV Blanquet, C Turleau, M S Gross-Morand, et al.
Pageof 5