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G Vaca

Showing results (51-60 of 74) with videos related to

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Human Genetics|January 1, 1981
Meiotic arrest at first spermatocyte level: a new inherited infertility disorderJ M Cantú, F Rivas, P Hernández-Jáuregui, et al.
Acta Paediatrica Scandinavica|January 1, 1980
Deficient cell immunity and mild intermittent hyperaminoacidemia in a patient with the Rubinstein-Taybi SyndromeF Rivas, R Fragoso, R Ramos-Zepeda, et al.
Ophthalmic Paediatrics and Genetics|November 1, 1987
Screening for red blood cell sorbitol dehydrogenase deficiency in patients with diabetes or cataractsC Medina, G Vaca, J Ríos, et al.
Genomics|March 1, 1995
Structural organization of the human sorbitol dehydrogenase gene (SORD)T Iwata, N C Popescu, D B Zimonjic, et al.
BMC Immunology|July 1, 2008
Environmental determinants of total IgE among school children living in the rural Tropics: importance of geohelminth infections and effect of anthelmintic treatmentPhilip J Cooper, Neal Alexander, Ana-Lucia Moncayo, et al.
Hemoglobin|January 1, 1981
Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican familiesB Ibarra, G Vaca, J M Cantú, et al.
Biology of the Neonate|January 1, 1989
Reduced levels of uridine diphosphate glucose pyrophosphorylase activity in fetal and neonatal human and guinea pig liverG Vaca, L P Castro-Félix, C Medina, et al.
Archivos De Investigacion Medica|January 1, 1978
Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiencyG Vaca, J Sanchez-Corona, C Medina, et al.
Boletin Medico Del Hospital Infantil De Mexico|September 1, 1990
[Effect of gene dosage on the glyceraldehyde-3-phosphate dehydrogenase enzyme (GAPD) in partial 12p13.3 pter trisomy]P Barros-Núñez, G Vaca, J Sánchez-Corona, et al.
Human Genetics|January 1, 1982
Red blood cell sorbitol dehydrogenase deficiency in a family with cataractsG Vaca, B Ibarra, M Bracamontes, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Human Genetics|January 1, 1981
Meiotic arrest at first spermatocyte level: a new inherited infertility disorderJ M Cantú, F Rivas, P Hernández-Jáuregui, et al.
Acta Paediatrica Scandinavica|January 1, 1980
Deficient cell immunity and mild intermittent hyperaminoacidemia in a patient with the Rubinstein-Taybi SyndromeF Rivas, R Fragoso, R Ramos-Zepeda, et al.
Ophthalmic Paediatrics and Genetics|November 1, 1987
Screening for red blood cell sorbitol dehydrogenase deficiency in patients with diabetes or cataractsC Medina, G Vaca, J Ríos, et al.
Genomics|March 1, 1995
Structural organization of the human sorbitol dehydrogenase gene (SORD)T Iwata, N C Popescu, D B Zimonjic, et al.
BMC Immunology|July 1, 2008
Environmental determinants of total IgE among school children living in the rural Tropics: importance of geohelminth infections and effect of anthelmintic treatmentPhilip J Cooper, Neal Alexander, Ana-Lucia Moncayo, et al.
Hemoglobin|January 1, 1981
Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican familiesB Ibarra, G Vaca, J M Cantú, et al.
Biology of the Neonate|January 1, 1989
Reduced levels of uridine diphosphate glucose pyrophosphorylase activity in fetal and neonatal human and guinea pig liverG Vaca, L P Castro-Félix, C Medina, et al.
Archivos De Investigacion Medica|January 1, 1978
Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiencyG Vaca, J Sanchez-Corona, C Medina, et al.
Boletin Medico Del Hospital Infantil De Mexico|September 1, 1990
[Effect of gene dosage on the glyceraldehyde-3-phosphate dehydrogenase enzyme (GAPD) in partial 12p13.3 pter trisomy]P Barros-Núñez, G Vaca, J Sánchez-Corona, et al.
Human Genetics|January 1, 1982
Red blood cell sorbitol dehydrogenase deficiency in a family with cataractsG Vaca, B Ibarra, M Bracamontes, et al.
Pageof 8