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Y S Shin

Showing results (1-10 of 204) with videos related to

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The Clinical Investigator|February 1, 1993
Diagnosis of fructose-1,6-bisphosphatase deficiency using leukocytes: normal leukocyte enzyme activity in three female patientsY S Shin
World Hospitals and Health Services : the Official Journal of the International Hospital Federation|December 9, 1994
Hospital accreditation--a universal perspectiveY S Shin
Journal of Inherited Metabolic Disease|January 1, 1990
Diagnosis of glycogen storage diseaseY S Shin
Fortschritte Der Medizin|June 20, 1990
[Prenatal diagnosis of genetic diseases]Y S Shin
European Journal of Pediatrics|January 1, 1995
Nucleotide sugars: determination of cellular levels and discrepancies in resultsY S Shin
Journal of Inherited Metabolic Disease|January 1, 1990
Cataract and metabolic diseaseW Endres, Y S Shin
European Journal of Pediatrics|May 1, 1995
Lens sorbitol dehydrogenase deficiency in a patient with congenital cataractV Vetter, Y S Shin
Bratislavske Lekarske Listy|January 7, 2005
Molecular and biochemical basis for variants and deficiency of GALT: report of 4 novel mutationsY S Shin, T Podskarbi
Taehan Kanho. the Korean Nurse|April 25, 1976
[Reports on demonstration projects for new health care delivery systems. II. Gangwha project]C O Jee, Y S Shin
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 25, 1980
Pitfalls in the radioactive method of galactose-1-phosphate uridyltransferase activity measurementY S Shin-Buehring, J Schaub
Pageof 21

Showing results (1-10 of 204) with videos related to

Sort By:
Pageof 21
The Clinical Investigator|February 1, 1993
Diagnosis of fructose-1,6-bisphosphatase deficiency using leukocytes: normal leukocyte enzyme activity in three female patientsY S Shin
World Hospitals and Health Services : the Official Journal of the International Hospital Federation|December 9, 1994
Hospital accreditation--a universal perspectiveY S Shin
Journal of Inherited Metabolic Disease|January 1, 1990
Diagnosis of glycogen storage diseaseY S Shin
Fortschritte Der Medizin|June 20, 1990
[Prenatal diagnosis of genetic diseases]Y S Shin
European Journal of Pediatrics|January 1, 1995
Nucleotide sugars: determination of cellular levels and discrepancies in resultsY S Shin
Journal of Inherited Metabolic Disease|January 1, 1990
Cataract and metabolic diseaseW Endres, Y S Shin
European Journal of Pediatrics|May 1, 1995
Lens sorbitol dehydrogenase deficiency in a patient with congenital cataractV Vetter, Y S Shin
Bratislavske Lekarske Listy|January 7, 2005
Molecular and biochemical basis for variants and deficiency of GALT: report of 4 novel mutationsY S Shin, T Podskarbi
Taehan Kanho. the Korean Nurse|April 25, 1976
[Reports on demonstration projects for new health care delivery systems. II. Gangwha project]C O Jee, Y S Shin
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 25, 1980
Pitfalls in the radioactive method of galactose-1-phosphate uridyltransferase activity measurementY S Shin-Buehring, J Schaub
Pageof 21