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G Vaca

Showing results (21-30 of 74) with videos related to

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Annales De Genetique|January 1, 1982
Sorbitol dehydrogenase (EC.1.1.1.14) polymorphism in human seminal plasmaB Ibarra, G Gonzalez-Quiroga, G Vaca, et al.
Blood|July 1, 1992
New glucose-6-phosphate dehydrogenase mutations from various ethnic groupsE Beutler, B Westwood, J T Prchal, et al.
Annales De Genetique|January 1, 1983
On the screening for inborn errors of galactose metabolismG Vaca, J Sànchez-Corona, N Olivares, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Membrane-bound sorbitol dehydrogenase in human red blood cells. Studies in normal subjects and in enzyme-deficient subjects with congenital cataractsA Alvarez, A Martínez, B Ibarra, et al.
Annales De Genetique|January 1, 1980
A simple assay for uridine diphosphate galactose 4-epimerase activityG Vaca, J Sanchez-Corona, N Olivares, et al.
Annales De Genetique|January 1, 1986
Bloom syndrome in a Mexican mestizo girlH Rivera, D García-Cruz, G Vaca, et al.
Annales De Genetique|January 1, 1985
Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segmentD García-Cruz, L García-Esquivel, H Rivera, et al.
Human Genetics|April 17, 1979
Los Angeles variant of galactose-1-phosphate uridyltransferase (EC 2.7.7.12) in a Mexican familyB Ibarra, G Vaca, J Sánchez-Corona, et al.
Clinical Genetics|June 1, 1987
Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomyH Rivera, L García-Esquivel, M Jiménez-Sáinz, et al.
Annales De Genetique|January 1, 1989
Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variantsB Ibarra, G Vaca, F J Perea, et al.
Pageof 8

Showing results (21-30 of 74) with videos related to

Sort By:
Pageof 8
Annales De Genetique|January 1, 1982
Sorbitol dehydrogenase (EC.1.1.1.14) polymorphism in human seminal plasmaB Ibarra, G Gonzalez-Quiroga, G Vaca, et al.
Blood|July 1, 1992
New glucose-6-phosphate dehydrogenase mutations from various ethnic groupsE Beutler, B Westwood, J T Prchal, et al.
Annales De Genetique|January 1, 1983
On the screening for inborn errors of galactose metabolismG Vaca, J Sànchez-Corona, N Olivares, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Membrane-bound sorbitol dehydrogenase in human red blood cells. Studies in normal subjects and in enzyme-deficient subjects with congenital cataractsA Alvarez, A Martínez, B Ibarra, et al.
Annales De Genetique|January 1, 1980
A simple assay for uridine diphosphate galactose 4-epimerase activityG Vaca, J Sanchez-Corona, N Olivares, et al.
Annales De Genetique|January 1, 1986
Bloom syndrome in a Mexican mestizo girlH Rivera, D García-Cruz, G Vaca, et al.
Annales De Genetique|January 1, 1985
Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segmentD García-Cruz, L García-Esquivel, H Rivera, et al.
Human Genetics|April 17, 1979
Los Angeles variant of galactose-1-phosphate uridyltransferase (EC 2.7.7.12) in a Mexican familyB Ibarra, G Vaca, J Sánchez-Corona, et al.
Clinical Genetics|June 1, 1987
Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomyH Rivera, L García-Esquivel, M Jiménez-Sáinz, et al.
Annales De Genetique|January 1, 1989
Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variantsB Ibarra, G Vaca, F J Perea, et al.
Pageof 8