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Japan Society of Human Genetics | 論文
- CHARACTERIZATION OF MARKER CHROMOSOMES BY FISH USING MICRODISSECTED PROBES FROM OLD CARNOY-FIXED CELLS : REPORT OF TWO CASES
- HIGH-RESOLUTION CHROMOSOME R-BANDING IN LYMPHOBLASTOID CELL LINES BY THE COMBINED USE OF CELL SYNCHRONIZATION AND ETHIDIUM BROMIDE TREATMENT
- ASSIGNMENT OF THE HUMAN GENE FOR KBF2/RBP-Jk TO CHROMOSOME 9p12-13 AND 9q13 BY FLUORESCENCE IN SITU HYBRIDIZATION
- MOLECULAR BASIS GOVERNING PRIMARY SEX IN MAMMALS
- NINE-bp REPEAT POLYMORPHISM IN EXON 1 OF THE hMSH3 GENE
- Carrier Detection of Werner′s Syndrome Using a Microsatellite That Exhibits Linkage Disequilibrium with the Werner′s Syndrome Locus
- TELOMERE SHORTENING IN PERIPHERAL BLOOD CELLS WAS RELATED WITH AGING BUT NOT WITH WHITE BLOOD CELL COUNT
- PCR-BASED GENOTYPING OF MNSs BLOOD GROUP : SUBTYPING OF M ALLELE TO M^G AND M^T
- Molecular Analysis of Xeroderma Pigmentosum Group A Gene(The Japan Society of Human Genetics Award Lecture)
- UNSTABLE EXPANSION OF TRIPLET REPEATS AS A NEW DISEASE MECHANISM FOR NEURODEGENERATIVE DISEASES
- Allotypes of the Fourth Component of Complement in Korean
- REEXAMINATION OF CHROMOSOMAL LOCI OF HUMAN MUSCLE ACTIN GENES BY FLUORESCENCE IN SITU HYBRIDIZATION
- A NOVEL AvaI POLYMORPHISM WITHIN EXON 5 OF THE RHODOPSIN GENE
- Detection of Monosomy 7 by Fluorescent In Situ Hybridization in Acute Nonlymphocytic Leukemia and Myelodysplastic Syndrome
- ITIH1^* Q0_, A NULL ALLELE OF INTER-ALPHA-TRYPSIN INHIBITOR H1 CAUSED BY DELETION/FRAMESHIFT MUTATION
- A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE GENE AMONG THE JAPANESE POPULATION
- AMELIORATION OF PROLIDASE DEFICIENCY IN FIBROBLASTS USING ADENOVIRUS MEDIATED GENE TRANSFER
- COSMIDS AND TRANSCRIBED SEQUENCES FROM CHROMOSOME 11q23
- Origin of the Adjacent 1 Disjunction
- An Improved Method for Genotyping of N-Acetyltransferase Polymorphism by Polymerase Chain Reaction