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T Gelbart

Showing results (11-20 of 81) with videos related to

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American Journal of Clinical Pathology|December 1, 1981
Falsely normal value in fluorometric transferase screening of galactosemic blood. A cautionary noteE Beutler, T Gelbart
Blood Cells, Molecules & Diseases|January 1, 1997
HLA-H mutations in the Ashkenazi Jewish populationE Beutler, T Gelbart
Blood Cells|January 1, 1986
The mechanism of removal of leukocytes by cellulose columnsE Beutler, T Gelbart
Human Genetics|February 1, 1994
Two new Gaucher disease mutationsE Beutler, T Gelbart
Blood Cells, Molecules & Diseases|June 6, 1998
Hematologically important mutations: Gaucher diseaseE Beutler, T Gelbart
Clinical and Laboratory Haematology|January 1, 1984
Globin-methionine complexes formed during labelling studiesE Beutler, T Gelbart
Annals of Human Genetics|May 1, 1990
Gaucher disease associated with a unique KpnI restriction site: identification of the amino-acid substitutionE Beutler, T Gelbart
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 24, 1990
The facile detection of the nt 1226 mutation of glucocerebrosidase by 'mismatched' PCRE Beutler, T Gelbart, C West
Molecular Medicine (Cambridge, Mass.)|June 1, 1997
HLA-H and associated proteins in patients with hemochromatosisE Beutler, C West, T Gelbart
Cell|July 13, 1990
Human red cell glucose-6-phosphate dehydrogenase: all active enzyme has sequence predicted by the X chromosome-encoded cDNAE Beutler, T Gelbart, W Kuhl
Pageof 9

Showing results (11-20 of 81) with videos related to

Sort By:
Pageof 9
American Journal of Clinical Pathology|December 1, 1981
Falsely normal value in fluorometric transferase screening of galactosemic blood. A cautionary noteE Beutler, T Gelbart
Blood Cells, Molecules & Diseases|January 1, 1997
HLA-H mutations in the Ashkenazi Jewish populationE Beutler, T Gelbart
Blood Cells|January 1, 1986
The mechanism of removal of leukocytes by cellulose columnsE Beutler, T Gelbart
Human Genetics|February 1, 1994
Two new Gaucher disease mutationsE Beutler, T Gelbart
Blood Cells, Molecules & Diseases|June 6, 1998
Hematologically important mutations: Gaucher diseaseE Beutler, T Gelbart
Clinical and Laboratory Haematology|January 1, 1984
Globin-methionine complexes formed during labelling studiesE Beutler, T Gelbart
Annals of Human Genetics|May 1, 1990
Gaucher disease associated with a unique KpnI restriction site: identification of the amino-acid substitutionE Beutler, T Gelbart
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 24, 1990
The facile detection of the nt 1226 mutation of glucocerebrosidase by 'mismatched' PCRE Beutler, T Gelbart, C West
Molecular Medicine (Cambridge, Mass.)|June 1, 1997
HLA-H and associated proteins in patients with hemochromatosisE Beutler, C West, T Gelbart
Cell|July 13, 1990
Human red cell glucose-6-phosphate dehydrogenase: all active enzyme has sequence predicted by the X chromosome-encoded cDNAE Beutler, T Gelbart, W Kuhl
Pageof 9