M. Iwata

发表

Identification of malignant hyperthermia-susceptible ryanodine receptor type 1 gene (RYR1) mutations in a child who died in a car after exposure to a high environmental temperature.

H. Nishio, A. Tamura, Koichi Suzuki, 2009, Legal medicine.

Postmortem molecular screening for cardiac ryanodine receptor type 2 mutations in sudden unexplained death: R420W mutated case with characteristics of status thymico-lymphatics.

H. Nishio, Koichi Suzuki, M. Iwata, 2006, Circulation journal : official journal of the Japanese Circulation Society.

Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene

L. Henke, J. Henke, H. Tsuji, 1996, Human Genetics.

Molecular basis for subtypic differences of the “a” subunit of coagulation factor XIII with description of the genesis of the subtypes

K. Matsui, Koichi Suzuki, Y. Mizoi, 1994, Human Genetics.

Sequence analysis of two de novo mutation alleles at the Y-STR locus

H. Nishio, A. Tamura, Koichi Suzuki, 2008 .

A de novo recombination in the ABO blood group gene and evidence for the occurrence of recombination products

K. Matsui, H. Tsuji, A. Tamura, 1997, Human Genetics.

A fatal case of amniotic fluid embolism with elevation of serum mast cell tryptase.

Akiyoshi Tamura, H. Nishio, K. Matsui, 2002, Forensic science international.

Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect.

H. Nishio, A. Tamura, Koichi Suzuki, 2012, Legal medicine.

Novel Polymorphisms in the Coding Sequence of the Coagulation Factor XIII A-Subunit and their Haplotype Diversity

L. Henke, J. Henke, H. Tsuji, 1996 .

Nucleotide Changes in Various Variants of the Coagulation Factor XIII A-Subunit

L. Henke, J. Henke, Koichi Suzuki, 1996 .

Identification of a novel mutation V2321M of the cardiac ryanodine receptor gene of sudden unexplained death and a phenotypic study of the gene mutations.

H. Nishio, A. Tamura, Koichi Suzuki, 2008, Legal medicine.

Sibling incest and formulation of paternity probability: case report.

H. Nishio, A. Tamura, T. Miyazaki, 2000, Legal medicine.

Genetic Polymorphisms of Human Complement Components in Japanese and Their Application to Parentage Testing

Koichi Suzuki, Y. Matsuo, H. Matsumoto, 1986 .

Traumatic basal subarachnoid hemorrhage suspected to have been caused by contrecoup cerebellar contusions: a case report.

H. Nishio, A. Tamura, Koichi Suzuki, 2014, Legal Medicine.

Postmortem molecular screening for mutations in ryanodine receptor type 1 (RYR1) gene in psychiatric patients suspected of having died of neuroleptic malignant syndrome.

H. Nishio, A. Tamura, Koichi Suzuki, 2010, Forensic science international.

Y Chromosomal Short Tandem Repeat Haplotypes in the Japanese Population

H. Nishio, A. Tamura, Koichi Suzuki, 2006, Journal of forensic sciences.

Analysis of two types of novel alleles in the DXS10011 locus.

H. Nishio, K. Matsui, A. Tamura, 2004, Legal medicine.

Sequence analysis of two de novo mutation alleles at the DXS10011 locus.

H. Nishio, K. Matsui, A. Tamura, 2003, Legal medicine.

Identification of newly polymorphic intron 40 markers of the von Willebrand factor gene in a Japanese population.

H. Nishio, A. Tamura, Koichi Suzuki, 2009, Legal medicine.

Allele 14 of vWA is characterized by 3′-flanking nucleotide substitutions and a TTAT insertion

H. Nishio, K. Matsui, H. Tsuji, 2003 .

Molecular Basis for Polymorphism of the “a” Subunit of Coagulation Factor XIII

A. Tamura, Koichi Suzuki, Y. Mizoi, 1994 .