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Japan Society of Human Genetics | 論文
- DISTRIBUTION OF ABO GENOTYPES AND ALLELE FREQUENCIES IN A KOREAN POPULATION
- Rapid Preparation of Diagnostic Probes for the Fragile X Syndrome by Direct PCR Amplification of Human Chromosomal DNA
- Sequence Tagged Sites of Microclones Obtained by Microdissection of a Human Chromosomal Region 11q23 and Isolation of Yeast Artificial Chromosomes
- Chromosome 1q Terminal Deletion Resulting from De Novo Translocation with an Acrocentric Chromosome
- ASSIGNMENT OF THE GENE ENCODING TYPE 1γ PROTEIN PHOSPHATASE CATALYTIC SUBUNIT (PPPlCC) ON HUMAN, RAT, AND MOUSE CHROMOSOMES
- BamHI Polymorphism in the Chinese,Malays and Indians in Singapore and Its Application in the Prenatal Diagnosis of β-Thalassemia
- HISTO-BLOOD GROUP LEWIS GENOTYPING FROM HUMAN HAIRS AND BLOOD
- A NOVEL SEQUENCE POLYMORPHISM IN EXON 8 OF THE HUMAN VITAMIN D-BINDING PROTEIN (GC) GENE IN AN AFRICAN POPULATION
- GM AND KM ALLOTYPES IN EIGHT TRIBAL POPULATIONS OF MADYHA PRADESH AND ORISSA INDIA
- Detection of Partial Deletion and Partial Duplication of Dystrophin Gene in Japanese Patients with Duchenne or Becker Muscular Dystrophy
- NcoI RESTRICTION FRAGMENT LENGTH POLYMORPHISM AT -308 OF THE TUMOR NECROSIS FACTOR ALPHA (TNFA) PROMOTER REGION IN KOREAN
- DUAL-COLOR FISH ANALYSIS OF BREAKPOINTS ON ROBERTSONIAN TRANSLOCATIONS
- SPINOCEREBELLAR ATAXIA 1 (SCA1) IN THE JAPANESE : ANALYSIS OF CAG TRINUCLEITIDE REPEAT EXPANSION AND INSTABILITY OF THE REPEAT FOR PATERNAL TRANSMISSION
- NONKETOTIC HYPERGLYCINEMIA : BIOCHEMICAL, MOLECULAR, AND NEUROLOGICAL ASPECTS
- DIRECT INSERTION OF EUCHROMATIC MATERIAL FROM CHROMOSOME Y IN THE X-CHROMOSOME IN HYPOGONADOTROPIC HYPOGONADISMS WITH CROHN'S DISEASE
- AN EcoRI RFLP IN HUMAN APC GENE
- ANALYSIS OF THE FIRST INTRON OF TNFB GENE BY NcoI RFLP IN KOREANS
- Dinucleotide Repeat Polymorphism at the D8S1055
- ROLES OF DNA REPAIR METHYLTRANSFERASE IN MUTAGENESIS AND CARCINOGENESIS
- MEGALOCORNEA-MENTAL RETARDATION SYNDROME : AN ADDITIONAL CASE REPORT