スポンサーリンク
Japan Society of Human Genetics | 論文
- TWO DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1218 AND D8S1219 LOCI
- TWO DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D8S1444 AND D8S1445 LOCI
- Construction of Radiation-Reduced Hybrids and their Use in Mapping of Microclones from Chromosome 10p11.2-q11.2
- BIPARENTAL ALLELES OF HLA-G ARE CO-DOMINANTLY EXPRESSED IN THE PLACENTA
- POLYMORPHIC AND TISSUE-SPECIFIC IMPRINTING OF THE HUMAN WILMS TUMOR GENE, WT1
- TWO POLYMORPHIC AvaI AND HhaI SITES IN A DIFFERENTIALLY METHYLATED REGION OF THE HUMAN H19 GENE
- THE GROWTH HORMONE RECEPTOR GENE MUTATION OF A JAPANESE PATIENT WITH LARON SYNDROME
- ASSIGNMENT OF THE HUMAN CONNEXIN43 GENE, GJA1, TO CHROMOSOME 6q22.3
- GENOMIC IMPRINTING AND ITS RELEVANCE TO GENETIC DISEASES
- 「ヒト細胞遺伝学命名に関する国際システム」1994年Menphis会議
- GENOTYPES OF ALDEHYDE DEHYDROGENASE AND ALCOHOL DEHYDROGENASE POLYMORPHISMS IN PATIENTS WITH LEBER'S HEREDITARY OPTIC NEUROPATHY
- MUTATIONS OF THE TYROSINASE GENE IN THREE KOREAN PATIENTS WITH TYPE I OCULOCUTANEOUS ALBINISM
- PREDOMINANCE OF THE MUTATION AT 1138 OF THE cDNA FOR THE FIBROBLAST GROWTH FACTOR RECEPTOR 3 IN JAPANESE PATIENTS WITH ACHONDROPLASIA
- FISH MAPPING OF A TRANSLOCATION BREAKPOINT AT 6q21 (OR q22) IN A PATIENT WITH HETEROTAXIA
- INCIDENCE OF PEROXISOMAL DISORDERS IN JAPAN
- Metacarpophalangeal Pattern Profile Analysis in 14 Japanese Children with Sotos Syndrome
- DINUCLEOTIDE REPEAT POLYMORPHISM IN 65k-GLUTAMATE DECARBOXYLASE GENE
- THREE JAPANESE PATIENTS WITH CRIGLER-NAJJAR SYNDROME TYPE I CARRY AN IDENTICAL NONSENSE MUTATION IN THE GENE FOR UDP-GLUCURONOSYLTRANSFERASE