Showing results (1-10 of 333) with videos related to
Sort By:
Pageof 34
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Newborn mass screening and molecular genetics of phenylketonuria in east AsiaY Okano, G IsshikiClinical Chemistry|June 6, 2000
Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate readerA Fujimoto, Y Okano, T Miyagi, et al.Journal of Human Genetics|May 13, 1999
Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patientsT Imamura, Y Okano, H Shintaku, et al.Journal of Inherited Metabolic Disease|January 1, 1986
Effects of phenylalanine loading on protein synthesis in the fetal heart and brain of rat: an experimental approach to maternal phenylketonuriaY Okano, I Z Chow, G Isshiki, et al.European Journal of Human Genetics : EJHG|November 26, 1999
Molecular basis for phenotypic heterogeneity in galactosaemia: prediction of clinical phenotype from genotype in Japanese patientsH Hirokawa, Y Okano, M Asada, et al.Journal of Human Genetics|November 26, 1999
Molecular characterization of galactokinase deficiency in Japanese patientsM Asada, Y Okano, T Imamura, et al.Human Genetics|December 22, 1998
Molecular characterization of phenylketonuria in Japanese patientsY Okano, M Asada, Y Kang, et al.Human Mutation|January 1, 1992
Frequency and distribution of phenylketonuric mutations in OrientalsY Okano, Y Hase, D H Lee, et al.Human Mutation|January 1, 1995
Molecular characterization of galactosemia (type 1) mutations in JapaneseJ Ashino, Y Okano, I Suyama, et al.Nihon Rinsho. Japanese Journal of Clinical Medicine|October 1, 1996
[Impaired glucose tolerance in the young]G IsshikiPageof 34