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I Yuasa

Showing results (91-100 of 98) with videos related to

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Human Biology|May 3, 2001
Geographical north-south decline in DNASE1*2 in Japanese populationsH Takeshita, T Yasuda, Y Nakashima, et al.
Clinical Genetics|May 3, 2014
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylationH Kodera, N Ando, I Yuasa, et al.
American Journal of Medical Genetics|March 9, 1999
Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cystH Zhang, T Yamamoto, E Nanba, et al.
Forensic Science International|May 1, 1993
Toxicological index of paraquat: a new strategy for assessment of severity of paraquat poisoning in 128 patientsJ Ikebuchi, A T Proudfoot, K Matsubara, et al.
Biochemistry and Molecular Biology International|October 24, 1998
Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and ChineseK Akaba, T Kimura, A Sasaki, et al.
Annals of Human Genetics|October 19, 2006
Distribution of the F374 allele of the SLC45A2 (MATP) gene and founder-haplotype analysisI Yuasa, K Umetsu, S Harihara, et al.
Biochemical Genetics|June 16, 2007
Distribution of two Asian-related coding SNPs in the MC1R and OCA2 genesI Yuasa, K Umetsu, S Harihara, et al.
Electrophoresis|October 24, 2001
Multiplex amplified product-length polymorphism analysis for rapid detection of human mitochondrial DNA variationsK Umetsu, M Tanaka, I Yuasa, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Human Biology|May 3, 2001
Geographical north-south decline in DNASE1*2 in Japanese populationsH Takeshita, T Yasuda, Y Nakashima, et al.
Clinical Genetics|May 3, 2014
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylationH Kodera, N Ando, I Yuasa, et al.
American Journal of Medical Genetics|March 9, 1999
Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cystH Zhang, T Yamamoto, E Nanba, et al.
Forensic Science International|May 1, 1993
Toxicological index of paraquat: a new strategy for assessment of severity of paraquat poisoning in 128 patientsJ Ikebuchi, A T Proudfoot, K Matsubara, et al.
Biochemistry and Molecular Biology International|October 24, 1998
Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and ChineseK Akaba, T Kimura, A Sasaki, et al.
Annals of Human Genetics|October 19, 2006
Distribution of the F374 allele of the SLC45A2 (MATP) gene and founder-haplotype analysisI Yuasa, K Umetsu, S Harihara, et al.
Biochemical Genetics|June 16, 2007
Distribution of two Asian-related coding SNPs in the MC1R and OCA2 genesI Yuasa, K Umetsu, S Harihara, et al.
Electrophoresis|October 24, 2001
Multiplex amplified product-length polymorphism analysis for rapid detection of human mitochondrial DNA variationsK Umetsu, M Tanaka, I Yuasa, et al.
Pageof 10