Duane Radial Ray Syndrome (Okihiro Syndrome) Maps to 20q13 and Results from Mutations in SALL4, a New Member of the SAL Family

Raidah Albaradie, Koki Yamada, Cynthia St. Hilaire, +9

The American Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathology +8

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2

Motoi Nakano, Koki Yamada, Jennifer Fain, +7

Nature Genetics

Extraocular MusclesHomozygous MutationsCongenital FibrosisDevelopmental BiologyGenetics +2

A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene

Motoi Nakano, Nobutomo Miwa, Akiyoshi Hirano, +2

BMC Genetics

A Consecutive Case Review of Orbital Blowout Fractures and Recommendations for Comprehensive Management

Hiroki Yano, Motoi Nakano, Kuniaki Anraku, +4

Plastic & Reconstructive Surgery

"Rogue" lymphocytes among Ukrainians not exposed to radioactive fall-out from the Chernobyl accident: the possible role of this phenomenon in oncogenesis, teratogenesis, and mutagenesis.

James V. Neel, A A Awa, Yuji Kodama, +2

Proceedings of the National Academy of Sciences

Radiation MedicineCytogeneticsUkrainian VillageExtreme Cytogenetic DamagePathogenesis +12

A method of preparing anisotropic Nd–Fe–B film magnets by pulsed laser deposition

Motoi Nakano, S. Sato, H. Fukunaga, +1

Journal of Applied Physics

Magnetic PropertiesEngineeringLaser DepositionHigh Deposition RateMagnetic Materials +18

Two missense mutations of the IRF6 gene in two Japanese families with popliteal pterygium syndrome

Noriko Matsuzawa, Shinji Kondo, Kazuo Shimozato, +6

American Journal of Medical Genetics Part A

Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family

Mitsuko Nakashima, Motoi Nakano, Akiyoshi Hirano, +5

Journal of Human Genetics

Genome-wide Linkage AnalysisGenetic DisorderJapanese FamilyGeneticsLinkage Analysis +6

Identification, characterization and mapping of the human ZIS (zinc-finger, splicing) gene

Motoi Nakano, K. Yoshiura, Masahiro Oikawa, +8

Gene

Human ZisGenetic DisorderGeneticsGene CharacterizationMolecular Genetics +6

Molecular mapping of a translocation breakpoint at 14q13 in a patient with mirror-image polydactyly of hands and feet

Naomichi Matsumoto, Hirofumi Ohashi, Rumiko Kato, +7

Human Genetics

Molecular MappingMolecular BiologyPathologyTranslocation BreakpointMirror-image Polydactyly