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H Ritter

Showing results (91-100 of 350) with videos related to

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Zentralblatt Fur Chirurgie|January 11, 1974
[Diagnostic aspects in retroperitoneal neurofibroma]G Endert, H Ritter, E Bindel
Humangenetik|January 1, 1975
Transspecific variability of red cell galactose 1-phosphate uridyl transferase in primatesS Bissbort, H Ritter, J Schmitt
Humangenetik|January 1, 1975
Transspecific variability of soluble glutamic-pyruvic transaminase in primatesJ Kömpf, H Ritter, J Schmitt
Humangenetik|January 1, 1973
Hereditary methemoglobinemia associated with NADH diaphorase deficiencyH Ritter, K Schmidt, J Schmitt
Human Genetics|March 1, 1990
Genetic studies on human thyroxine-binding globulin (TBG)C Luckenbach, J Kömpf, H Ritter
American Journal of Surgery|October 29, 2010
Trauma to the abdomenH H RITTER, B B KAYE
Human Genetics|January 1, 1980
Substrate affinity in PGM1, PGM2, and PGM2 isozymesG Siebert, H Ritter, J Kömpf
Human Genetics|January 1, 1980
Galactose-1-phosphate-uridyltransferase (E.C. 2.7.7.11): a simple routine method for detecting individuals heterozygous for the silent allele Gt 0G Siebert, J Kömpf, H Ritter
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|September 1, 1979
[Isotope methods in the diagnosis of venous disease. II. Results of radionuclide venography (author's transl)]G Endert, H Ritter, E Schumann
Seminars in Diagnostic Pathology|November 14, 2016
Pulmonary and pleural pathology: Contributions of Dr. Louis "Pepper" DehnerJon H Ritter, D Ashley Hill
Pageof 35

Showing results (91-100 of 350) with videos related to

Sort By:
Pageof 35
Zentralblatt Fur Chirurgie|January 11, 1974
[Diagnostic aspects in retroperitoneal neurofibroma]G Endert, H Ritter, E Bindel
Humangenetik|January 1, 1975
Transspecific variability of red cell galactose 1-phosphate uridyl transferase in primatesS Bissbort, H Ritter, J Schmitt
Humangenetik|January 1, 1975
Transspecific variability of soluble glutamic-pyruvic transaminase in primatesJ Kömpf, H Ritter, J Schmitt
Humangenetik|January 1, 1973
Hereditary methemoglobinemia associated with NADH diaphorase deficiencyH Ritter, K Schmidt, J Schmitt
Human Genetics|March 1, 1990
Genetic studies on human thyroxine-binding globulin (TBG)C Luckenbach, J Kömpf, H Ritter
American Journal of Surgery|October 29, 2010
Trauma to the abdomenH H RITTER, B B KAYE
Human Genetics|January 1, 1980
Substrate affinity in PGM1, PGM2, and PGM2 isozymesG Siebert, H Ritter, J Kömpf
Human Genetics|January 1, 1980
Galactose-1-phosphate-uridyltransferase (E.C. 2.7.7.11): a simple routine method for detecting individuals heterozygous for the silent allele Gt 0G Siebert, J Kömpf, H Ritter
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|September 1, 1979
[Isotope methods in the diagnosis of venous disease. II. Results of radionuclide venography (author's transl)]G Endert, H Ritter, E Schumann
Seminars in Diagnostic Pathology|November 14, 2016
Pulmonary and pleural pathology: Contributions of Dr. Louis "Pepper" DehnerJon H Ritter, D Ashley Hill
Pageof 35