Umetsu Kazuo | Department Of Legal Medicine Yamagata University School Of Medicine

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概要

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著作論文

Molecular basis of complement factor I (CFI) polymorphism : one of two polymorphic suballeles responsible for CFI A is Japanese-specific
OCA2^*481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations
Molecular characterization of four alpha-l-antitrypsin variant alleles found in Japanese population : a mutation hot spot at the codon for amino acid 362
Characterization of genomic rearrangements of the α_1-acid glycoprotein/orosomucoid gene in Ghanaians
A new single-nucleotide polymorphism in the seventh component of complement (C7) gene
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
ITIH1^* Q0_, A NULL ALLELE OF INTER-ALPHA-TRYPSIN INHIBITOR H1 CAUSED BY DELETION/FRAMESHIFT MUTATION
東アジア4集団におけるalpha-2-HS-glycoprotein型の分布〔英文〕
Y-chromosomal STR haplotyping in a Japanese population
Population Genetic Studies on Nine Aboriginal Ethnic Groups of Taiwan, II. Serum Protein Systems
A Japanese-specific allele in the GALNT11 gene

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