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

T Gelbart

Showing results (1-10 of 81) with videos related to

Pageof 9
Sort By:
Blood Cells, Molecules & Diseases|August 22, 2000
A common intron 3 mutation (IVS3 -48c-->g) leads to misdiagnosis of the c.845G-->A (C282Y) HFE gene mutationE Beutler, T Gelbart
Human Mutation|January 1, 1996
Glucocerebrosidase (Gaucher disease)E Beutler, T Gelbart
American Journal of Medical Genetics|October 1, 1992
Mutation analysis in Gaucher diseaseE Beutler, T Gelbart
Human Mutation|January 1, 1994
Erroneous assignment of Gaucher disease genotype as a consequence of a complete gene deletionE Beutler, T Gelbart
The Journal of Laboratory and Clinical Medicine|May 1, 1985
Plasma glutathione in health and in patients with malignant diseaseE Beutler, T Gelbart
Genetic Testing|August 23, 2000
Large-scale screening for HFE mutations: methodology and costE Beutler, T Gelbart
British Journal of Haematology|October 1, 1993
Gaucher disease mutations in non-Jewish patientsE Beutler, T Gelbart
Blood Cells, Molecules & Diseases|January 1, 1997
Hematologically important mutations: Gaucher diseaseE Beutler, T Gelbart
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1986
Improved assay of the enzymes of glutathione synthesis: gamma-glutamylcysteine synthetase and glutathione synthetaseE Beutler, T Gelbart
Blood|May 29, 2000
Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white populationE Beutler, T Gelbart
Pageof 9

Showing results (1-10 of 81) with videos related to

Sort By:
Pageof 9
Blood Cells, Molecules & Diseases|August 22, 2000
A common intron 3 mutation (IVS3 -48c-->g) leads to misdiagnosis of the c.845G-->A (C282Y) HFE gene mutationE Beutler, T Gelbart
Human Mutation|January 1, 1996
Glucocerebrosidase (Gaucher disease)E Beutler, T Gelbart
American Journal of Medical Genetics|October 1, 1992
Mutation analysis in Gaucher diseaseE Beutler, T Gelbart
Human Mutation|January 1, 1994
Erroneous assignment of Gaucher disease genotype as a consequence of a complete gene deletionE Beutler, T Gelbart
The Journal of Laboratory and Clinical Medicine|May 1, 1985
Plasma glutathione in health and in patients with malignant diseaseE Beutler, T Gelbart
Genetic Testing|August 23, 2000
Large-scale screening for HFE mutations: methodology and costE Beutler, T Gelbart
British Journal of Haematology|October 1, 1993
Gaucher disease mutations in non-Jewish patientsE Beutler, T Gelbart
Blood Cells, Molecules & Diseases|January 1, 1997
Hematologically important mutations: Gaucher diseaseE Beutler, T Gelbart
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1986
Improved assay of the enzymes of glutathione synthesis: gamma-glutamylcysteine synthetase and glutathione synthetaseE Beutler, T Gelbart
Blood|May 29, 2000
Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white populationE Beutler, T Gelbart
Pageof 9