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 Dubourg

Showing results (1-10 of 28) with videos related to

Pageof 3
Sort By:
Human Genetics|December 22, 1998
FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variantM Blayau, S Odent, C Dubourg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Blood-borne seeding by hematopoietic and endothelial precursors from the allantoisA Caprioli, T Jaffredo, R Gautier, et al.
Bulletin De La Societe De Pathologie Exotique Et De Ses Filiales|January 1, 1986
[Malaria in Gabon. I. Study of 500 children with fever in Libreville]D Richard-Lenoble, M Kombila, J Chandenier, et al.
Human Mutation|March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. OnlineC Dubourg, S Odent, P Fergelot, et al.
Atherosclerosis|February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patientsI Dorval, P Jezequel, C Dubourg, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.
Journal of Medical Genetics|January 7, 2005
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutationsL Pasquier, C Dubourg, M Gonzales, et al.
Annales De Biologie Clinique|January 9, 2004
[Genetic study of holoprosencephaly]C Dubourg, L Lazaro, M Blayau, et al.
Cytogenetics and Cell Genetics|April 25, 2000
Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseasesL Guenet, C Henry, B Toutain, et al.
Clinical Chemistry|December 1, 1994
Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic populationI Dorval, P Fergelot, C Dubourg, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Human Genetics|December 22, 1998
FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variantM Blayau, S Odent, C Dubourg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Blood-borne seeding by hematopoietic and endothelial precursors from the allantoisA Caprioli, T Jaffredo, R Gautier, et al.
Bulletin De La Societe De Pathologie Exotique Et De Ses Filiales|January 1, 1986
[Malaria in Gabon. I. Study of 500 children with fever in Libreville]D Richard-Lenoble, M Kombila, J Chandenier, et al.
Human Mutation|March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. OnlineC Dubourg, S Odent, P Fergelot, et al.
Atherosclerosis|February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patientsI Dorval, P Jezequel, C Dubourg, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephalyL Pasquier, C Dubourg, M Blayau, et al.
Journal of Medical Genetics|January 7, 2005
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutationsL Pasquier, C Dubourg, M Gonzales, et al.
Annales De Biologie Clinique|January 9, 2004
[Genetic study of holoprosencephaly]C Dubourg, L Lazaro, M Blayau, et al.
Cytogenetics and Cell Genetics|April 25, 2000
Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseasesL Guenet, C Henry, B Toutain, et al.
Clinical Chemistry|December 1, 1994
Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic populationI Dorval, P Fergelot, C Dubourg, et al.
Pageof 3