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 H Lindenbaum

Showing results (51-60 of 56) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 56 results.
American Journal of Medical Genetics|April 1, 1992
Molecular studies of the fragile X syndromeS J Knight, M C Hirst, A Roche, et al.
Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MSR A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)|April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduriaJ Boué, R A Chalmers, B M Tracey, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complexA O Wilkie, H C Zeitlin, R H Lindenbaum, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
American Journal of Medical Genetics|April 1, 1992
Molecular studies of the fragile X syndromeS J Knight, M C Hirst, A Roche, et al.
Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MSR A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)|April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduriaJ Boué, R A Chalmers, B M Tracey, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complexA O Wilkie, H C Zeitlin, R H Lindenbaum, et al.
Pageof 6