スポンサーリンク
Japan Society of Human Genetics | 論文
- Point Mutations of Rhodopsin Gene Found in Japanese Families with Autosomal Dominant Retinitis Pigmentosa(ADRP)
- Assignment of the Human Cytochrome P-450 Nifedipine Oxidase Gene(CYP3A4)to Chromosome 7 at Band q22.1 by Fluorescence In Situ Hybridization
- LONG Y-ASSOCIATED (GATA)_n ALLELES WERE OBSERVED IN A FEW ETHNIC GROUPS IN ASIA
- Expression of the Tn Antigen on Erythroid Cells from a Patient with Tn Syndrome
- A Case of Atypical Duchenne Type Muscular Dystrophy with Fragile X
- MET 235 THR POLYMORPHISM OF ANGIOTENSINOGEN IN INDONESIANS
- Cytogenetic Study of a Severe Case of Pallister-Killian Syndrome Using Fluorescence In Situ Hybridization
- APPLICATION OF DNA MARKERS TO CLINICAL GENETICS
- A Linkage Study with DNA Markers(D4S95,D4S115,and D4S111)in Japanese Huntington Disease Families
- OVERVIEW OF THE HUMAN GENOME PROJECT IN JAPAN
- Chromosome Abnormalities and Rare Fragile Sites Detected in Azoospermia Patients
- G-Banding Analysis of Radiation-Induced Chromosome Damage in Lymphocytes of Hiroshima A-Bomb Survivors
- The Costello Syndrome--Report of a Case and Review of the Literature
- ANAL ATRESIA : EFFECT OF SMOKING AND DRINKING HABITS DURING PREGNANCY
- The Costello Syndrome--A Boy with Thick Mitral Valves and Arrythmias
- Genetic Polymorphism of Human Factor H(HF,β1H Globulin)in Chinese Han Population in Northeast China
- O-Gene Detection by Allele Specific Amplification in the ABO Blood Group System
- 名誉会員Erik Essen-Moller教授を悼む
- ALLELIC FREQUENCIES OF TWELVE DINUCLEOTIDE REPEAT MARKER LOCI ON CHROMOSOME 13 IN THE NORMAL JAPANESE POPULATION
- MOLECULAR CHARACTERIZATION OF AN UNUSUAL VARIANT OF THE SHORT ARM OF CHROMOSOME 15 BY FISH-TECHNIQUE