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Legal Medicine (Tokyo, Japan)|April 30, 2008
Haplotype analysis of seven Y-STRs (eleven loci) in two Japanese populationsIsao Yuasa, Yoshito Irizawa, Hiroaki Nakamura, et al.
Brain & Development|September 18, 2003
Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type IaHiroaki Ono, Nobuo Sakura, Katsuko Yamashita, et al.
Legal Medicine (Tokyo, Japan)|August 7, 2016
Genotyping of the c.1423C>T (p.P475S) polymorphism in the ADAMTS13 gene by APLP and HRM assays: Northeastern Asian origin of the mutantMayumi Nakagawa, Aya Matsusue, Kazuo Umetsu, et al.
Human Biology|October 16, 2004
Molecular basis of ESD*5 and ESD*7 and haplotype analysis with new polymorphisms in intronsIsao Yuasa, Kazuo Umetsu, Shuichi Tsuchida, et al.
International Journal of Legal Medicine|September 30, 2004
MATP polymorphisms in Germans and Japanese: the L374F mutation as a population marker for CaucasoidsIsao Yuasa, Kazuo Umetsu, Gotaro Watanabe, et al.
Legal Medicine (Tokyo, Japan)|December 4, 2012
A hypervariable STR polymorphism in the CFI gene: mutation rate and no linkage disequilibrium with FGAIsao Yuasa, Nori Nakayashiki, Kazuo Umetsu, et al.
Biochemical Genetics|May 4, 2006
The structure and diversity of alpha1-acid glycoprotein/orosomucoid gene in AfricansIsao Yuasa, Hiroaki Nakamura, Kazuo Umetsu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 12, 2008
Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylationTohru Okanishi, Yoshiaki Saito, Isao Yuasa, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 2006
Variation of interleukin 8 -251 A>T polymorphism in worldwide populations and intra-ethnic differences in Japanese populationsJunko Fujihara, Kuninori Shiwaku, Toshihiro Yasuda, et al.
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