スポンサーリンク
Japan Society of Human Genetics | 論文
- Apolipoprotein E5 and E7 in Apparently Healthy Japanese Males--Frequencies and Relation to Plasma Lipid Levels
- MOLECULAR BASIS OF ZELLWEGER SYNDROME, β-KETOTHIOLASE DEFICIENCY AND MUCOPOLYSACCHARIDOSES
- DNA Analysis of Two Patients with a Non-Fluorescent Y Chromosome
- The Costello Syndrome--Are Nasal Papillomata Essential?
- Partial Monosomy 5p and Partial Trisomy 5q due to Paternal Pericentric Inversion of Chromosome 5
- A CONVENIENT METHOD FOR GENOTYPING OF HUMAN O^6-METHYLGUANINE-DNA METHYLTRANSFERASE POLYMORPHISM
- 名誉会員半田順俊氏の逝去を悼む
- Physical Parameters in Japanese Newborns
- Isolation of 2 Novel RFLP Markers and Their Localization at 2q35 by Microdissection and Subsequent Enzymatic Amplification
- A PATIENT WITH SCHINZEL-GIEDION SYNDROME AND A REVIEW OF 20 PATIENTS
- Isolation and Characterization of a DNA Fragment Containing Various Kinds of Repetitive Sequences Located on Human Chromosome 21
- A Case of Goldenhar Syndrome Associated with Growth Hormone Deficiency
- Restriction Fragment Length Polymorphisms of the CYP11B1 Gene in the Japanese Population
- Asphyxiating thoracic dystrophy--Surgical Correction and 2-Year follow-up in a Girl
- Terminal Deletion of the Short Arm of Chromosome 3
- Sexing of In Vitro-Fertilized Preimplantation Mouse Embryos by the PCR Method
- MEVALONIC ACIDEMIA : FIRST CASE OF JAPAN
- A Chromosome Painting Method for Human Sperm Chromosomes Using Fluorescent In Situ Hybridization
- A NOVEL (CA)_n POLYMORPHISM ON 6p21.1-21.2
- Genetic Heterogeneity of Dominantly Inherited Olivopontocerebellar Atrophy(OPCA) in the Japanese--Linkage Study of Two Pedigrees and Evidence for the Disease Locus on Chromosome 12q(SCA2)