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

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Electrophoresis|December 30, 2004
Multiplex amplified product-length polymorphism analysis of 36 mitochondrial single-nucleotide polymorphisms for haplogrouping of East Asian populationsKazuo Umetsu, Masashi Tanaka, Isao Yuasa, et al.
Legal Medicine (Tokyo, Japan)|June 16, 2010
A Japanese-specific allele in the GALNT11 geneIsao Yuasa, Kazuo Umetsu, Aya Matsusue, et al.
Legal Medicine (Tokyo, Japan)|February 15, 2011
Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European, and African populationsTomonori Muro, Reiko Iida, Junko Fujihara, et al.
Electrophoresis|July 20, 2011
Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2Haruo Takeshita, Junko Fujihara, Mikiko Soejima, et al.
Legal Medicine (Tokyo, Japan)|August 10, 2015
The global distribution of the p.R1193Q polymorphism in the SCN5A geneAya Matsusue, Isao Yuasa, Kazuo Umetsu, et al.
Journal of Human Genetics|June 15, 2007
OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populationsIsao Yuasa, Kazuo Umetsu, Shinji Harihara, et al.
JIMD Reports|February 23, 2013
Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass SpectrometryToshiyuki Fukao, Shinsuke Maruyama, Toshihiro Ohura, et al.
Journal of Human Genetics|October 1, 2008
Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specificIsao Yuasa, Mayumi Nakagawa, Kazuo Umetsu, et al.
Journal of Inherited Metabolic Disease|March 25, 2011
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type IMailys Guillard, Yoshinao Wada, Hana Hansikova, et al.
Human Mutation|October 12, 2013
De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathyHirofumi Kodera, Kazuyuki Nakamura, Hitoshi Osaka, et al.
Pageof 6