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

R V Lebo

Showing results (71-80 of 84) with videos related to

Pageof 9
Sort By:
American Journal of Medical Genetics|March 1, 1994
Prenatal diagnosis of unusual hemoglobinopathiesJ H Kim, R V Lebo, S P Cai, et al.
American Journal of Medical Genetics|June 1, 1993
Mental retardation locus in Xp21 chromosome microdeletionM H Fries, R V Lebo, S A Schonberg, et al.
American Journal of Human Genetics|August 1, 2000
Rare etiology of autosomal recessive disease in a child with noncarrier parentsR V Lebo, L R Shapiro, E Y Fenerci, et al.
American Journal of Medical Genetics|October 23, 1995
Asian hereditary neuropathy patients with peripheral myelin protein-22 gene aneuploidyA Ohnishi, L Y Li, Y Fukushima, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomyF P Thomas, T J Geller, A F Hahn, et al.
Biochemical and Biophysical Research Communications|November 30, 1992
Isolation and characterization of Y chromosome DNA probesS B Farah, D C Gruenert, J A Lepercq, et al.
The Journal of Clinical Investigation|December 1, 1986
cDNA cloning of human plasminogen activator-inhibitor from endothelial cellsD Ginsburg, R Zeheb, A Y Yang, et al.
Human Genetics|January 1, 1982
Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sortingR V Lebo, Y W Kan, M C Cheung, et al.
American Journal of Medical Genetics|September 1, 1993
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridizationR V Lebo, L Martelli, Y Su, et al.
American Journal of Medical Genetics|December 15, 1993
Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategiesE S Mansfield, J M Robertson, R V Lebo, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|March 1, 1994
Prenatal diagnosis of unusual hemoglobinopathiesJ H Kim, R V Lebo, S P Cai, et al.
American Journal of Medical Genetics|June 1, 1993
Mental retardation locus in Xp21 chromosome microdeletionM H Fries, R V Lebo, S A Schonberg, et al.
American Journal of Human Genetics|August 1, 2000
Rare etiology of autosomal recessive disease in a child with noncarrier parentsR V Lebo, L R Shapiro, E Y Fenerci, et al.
American Journal of Medical Genetics|October 23, 1995
Asian hereditary neuropathy patients with peripheral myelin protein-22 gene aneuploidyA Ohnishi, L Y Li, Y Fukushima, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomyF P Thomas, T J Geller, A F Hahn, et al.
Biochemical and Biophysical Research Communications|November 30, 1992
Isolation and characterization of Y chromosome DNA probesS B Farah, D C Gruenert, J A Lepercq, et al.
The Journal of Clinical Investigation|December 1, 1986
cDNA cloning of human plasminogen activator-inhibitor from endothelial cellsD Ginsburg, R Zeheb, A Y Yang, et al.
Human Genetics|January 1, 1982
Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sortingR V Lebo, Y W Kan, M C Cheung, et al.
American Journal of Medical Genetics|September 1, 1993
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridizationR V Lebo, L Martelli, Y Su, et al.
American Journal of Medical Genetics|December 15, 1993
Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategiesE S Mansfield, J M Robertson, R V Lebo, et al.
Pageof 9