Showing results (51-60 of 74) with videos related to
Sort By:
Pageof 8
Journal of Human Genetics|June 11, 1998
A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemiaS Kure, T Shinka, Y Sakata, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 30, 1985
Altered metabolic profiles of valproic acid in a patient with Reye's syndromeT Kuhara, Y Inoue, M Matsumoto, et al.Journal of Human Genetics|June 11, 1998
Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsyS Kure, Y Sakata, S Miyabayashi, et al.Hinyokika Kiyo. Acta Urologica Japonica|December 1, 1989
[Occupational uroepithelial cancer: current status in Wakayama city and clinical study]S Morimoto, Y Uekado, H Aoshi, et al.Biomedical Mass Spectrometry|December 1, 1981
Application of a gas chromatography mass spectrometry computer system for clinical diagnosisT Mizuno, N Abe, H Teshima, et al.Hinyokika Kiyo. Acta Urologica Japonica|June 1, 1987
[Uroepithelial tumors of the upper urinary tract following bladder cancer]T Shinka, S Morimoto, Y Uekado, et al.Journal of Human Genetics|April 3, 2001
Y chromosome compound haplotypes with the microsatellite markers DXYS265, DXYS266, and DXYS241J Lee, S E Kotliarova, A A Ewis, et al.Acta Paediatrica Japonica : Overseas Edition|April 1, 1992
GC/MS analysis of urine in 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyT Shinka, T Kuhara, Y Inoue, et al.Neurology|September 26, 1997
Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescenceH Miyajima, K E Orii, Y Shindo, et al.Journal of Human Genetics|July 14, 2001
Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemiaS Kure, K Kojima, T Kudo, et al.Pageof 8