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 Hamel

Showing results (81-90 of 291) with videos related to

Pageof 30
Sort By:
Human Molecular Genetics|August 1, 1992
Improving the polymorphism content of the 3' UTR of the human IGF2R geneF A Hol, M P Geurds, B C Hamel, et al.
The Journal of Experimental Medicine|July 1, 1993
Molecular characterization of two human autoantigens: unique cDNAs encoding 95- and 160-kD proteins of a putative family in the Golgi complexM J Fritzler, J C Hamel, R L Ochs, et al.
Neurotoxicology and Teratology|March 1, 1991
Maternal cocaine use and infant behaviorD R Neuspiel, S C Hamel, E Hochberg, et al.
Journal Francais D'Ophtalmologie|May 31, 2011
[Screening for retinal detachment using wide-field retinal imaging]G Bonnay, F Nguyen, I Meunier, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|November 1, 1993
[Pathologic Doppler flowmetry of the uterine artery and histologic changes of the placenta]C Hamel-Desnos, J M Allart, E Leconte, et al.
Human Mutation|January 1, 1996
A novel mutation (S558X) causing choroideremiaL Beaufrère, S Tuffery, C Hamel, et al.
The Journal of Clinical Investigation|January 1, 1991
Molecular definition and sequence motifs of the 52-kD component of human SS-A/Ro autoantigenE K Chan, J C Hamel, J P Buyon, et al.
Seminars in Nuclear Medicine|March 2, 2019
Knowledge Synthesis in Evidence-Based MedicineC Garritty, A Stevens, C Hamel, et al.
Human Mutation|June 22, 2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosaC Bareil, V Delague, B Arnaud, et al.
Journal of Medical Genetics|October 10, 1997
Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndromeP Rump, B C Hamel, A J Pinckers, et al.
Pageof 30

Showing results (81-90 of 291) with videos related to

Sort By:
Pageof 30
Human Molecular Genetics|August 1, 1992
Improving the polymorphism content of the 3' UTR of the human IGF2R geneF A Hol, M P Geurds, B C Hamel, et al.
The Journal of Experimental Medicine|July 1, 1993
Molecular characterization of two human autoantigens: unique cDNAs encoding 95- and 160-kD proteins of a putative family in the Golgi complexM J Fritzler, J C Hamel, R L Ochs, et al.
Neurotoxicology and Teratology|March 1, 1991
Maternal cocaine use and infant behaviorD R Neuspiel, S C Hamel, E Hochberg, et al.
Journal Francais D'Ophtalmologie|May 31, 2011
[Screening for retinal detachment using wide-field retinal imaging]G Bonnay, F Nguyen, I Meunier, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|November 1, 1993
[Pathologic Doppler flowmetry of the uterine artery and histologic changes of the placenta]C Hamel-Desnos, J M Allart, E Leconte, et al.
Human Mutation|January 1, 1996
A novel mutation (S558X) causing choroideremiaL Beaufrère, S Tuffery, C Hamel, et al.
The Journal of Clinical Investigation|January 1, 1991
Molecular definition and sequence motifs of the 52-kD component of human SS-A/Ro autoantigenE K Chan, J C Hamel, J P Buyon, et al.
Seminars in Nuclear Medicine|March 2, 2019
Knowledge Synthesis in Evidence-Based MedicineC Garritty, A Stevens, C Hamel, et al.
Human Mutation|June 22, 2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosaC Bareil, V Delague, B Arnaud, et al.
Journal of Medical Genetics|October 10, 1997
Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndromeP Rump, B C Hamel, A J Pinckers, et al.
Pageof 30