スポンサーリンク
Department of Genetics, Institute for Developmental Research, Aichi Human Service Center | 論文
- Polymorphism of Extracellular Superoxide Dismutase(EC-SOD) Gene : Relation to the Mutation Responsible for High EC-SOD Level in Serum.
- POLYMORPHISM OF EXTRACELLULAR SUPEROXIDE DISMUTASE (EC-SOD) GENE : RELATION TO THE MUTATION RESPONSIBLE FOR HIGH EC-SOD LEVEL IN SERUM
- A NOVEL DE NOVO MUTATION IN HPRT GENE RESPONSIBLE FOR LESCH-NYHAN SYNDROME (HPRT_)
- Mutation in the gene encoding the fibroblast growth factor receptor-3 in Korean children with achondroplasia
- Molecular analysis of extracellular-superoxide dismutase gene associated with high level in serum.
- MOLECULAR ANALYSIS OF EXTRACELLULAR-SUPEROXIDE DISMUTASE GENE ASSOCIATED WITH HIGH LEVEL IN SERUM
- Scheie syndrome (MPS-IS) presented as bilateral trigger thumb
- Meiotic segregation of the inversion X chromosome in Chinese hamsters : Papers Presented from Platform
- Establishment and karyological analysis of embryonic stem cell stock in the Chinese hamster
- Painting of Chinese hamster chromosomes with chromosome specific probes constructed by microdissection and sorting
- No interchromosomal effect at meiosis in male Chinese hamsters heterozygous for reciprocal translocations : Abstracts of Papers Presented at the Thirtieth Annual Meeting of the Japanese Teratology Society Miyazaki, Japan, July 12-13, 1990
- Developmental abnormalities of chromosomally unbalanced fetuses in the Chinese hamster : Abstracts of Papers Presented at the Thirty-First Annual Meeting of the Japanese Teratology Society Izumo, Japan, July 11-12, 1991
- Meiotic crossing-over on the interstitial segments in male Chinese hamsters heterozygous for single and double reciprocal translocatrions
- MS-3 Mutant Mice and Human Diseases Associated with Defective Myosin Genes.(HUMAN CONGENITAL ANOMALIES AND ANIMAL MODELS)
- C-03 The Structure of Mouse Myosin X and Chromosomal Assignment of its Gene.
- E-4 The organization of Chinese hamster chromosomes based on cytogenetic mapping of cosmid markers.
- C-04 Construction of Chromosome Map of Cosmid Clones Isolated from a Genomic Library of the Chinese Hamster.
- DNA Haplotype Analysis at the Phenylalanine Hydroxynase Locus in Japanese Families
- Investigation on the storage of heavy metals in human fetuses and mothers
- Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation