|
MeSH term |
Japanese |
Link |
01 |
|
|
Chromosomes, Human, Pair 19
|
ヒト第19染色体
|
|
|
|
|
Protein Modification, Translational
|
翻訳蛋白質修飾
|
|
|
|
|
Genes, Dominant
|
優性遺伝子
|
|
|
|
|
Haplotypes
|
ハプロタイプ
|
|
|
|
|
Genetic Markers
|
遺伝子マーカー
|
|
|
|
|
Metabolic Clearance Rate
|
代謝クリアランス
|
|
|
|
|
Medical Records
|
診療録
|
|
|
|
|
Retrospective Studies
|
後向き研究
|
|
|
|
|
Protein Processing, Post-Translational
|
翻訳後蛋白質プロセシング
|
|
|
|
|
Lod Score
|
ロッドスコア
|
|
|
|
|
Founder Effect
|
創始者効果
|
|
|
|
|
Glycosylation
|
-
|
|
|
|
|
Codon, Nonsense
|
ナンセンスコドン
|
|
|
|
|
Chromosomes, Human, Pair 6
|
ヒト第6染色体
|
|
|
|
|
Alternative Splicing
|
選択的スプライシング
|
|
|
|
|
Genetic Linkage
|
連鎖(遺伝学)
|
|
|
|
|
Mass Screening
|
集団検診
|
|
|
|
|
Germ-Line Mutation
|
生殖細胞系変異
|
|
|
|
|
Fatal Outcome
|
致死的転帰
|
|
|
|
|
Amino Acid Substitution
|
アミノ酸置換
|
|
|
|
|
Risk Factors
|
危険因子
|
|
|
|
|
Sequence Homology, Amino Acid
|
アミノ酸配列相同性
|
|
|
|
|
Genetic Variation
|
遺伝的多様性
|
|
|
|
|
Genetic Testing
|
遺伝学的スクリーニング
|
|
|
|
|
Mutation, Missense
|
ミスセンス変異
|
|
|
|
|
Chromosome Aberrations
|
染色体異常
|
|
|
|
|
Prevalence
|
有病率
|
|
|
|
|
Point Mutation
|
点変異
|
|
|
|
|
Cohort Studies
|
コホート研究
|
|
|
|
|
Mutation
|
変異
|
|
|
|
|
Polymorphism, Genetic
|
遺伝子多型
|
|
|
|
|
Follow-Up Studies
|
追跡研究
|
|
|
|
|
Base Sequence
|
塩基配列
|
|
|
|
|
Amino Acid Sequence
|
アミノ酸配列
|
|
|
|
|
Phenotype
|
表現型
|
|
|
