|
MeSH term |
Japanese |
Link |
01 |
|
|
X Chromosome
|
X染色体
|
|
|
|
|
Genetic Linkage
|
連鎖(遺伝学)
|
|
|
|
|
Chromosome Deletion
|
染色体欠失
|
|
|
|
|
Sex Chromosome Aberrations
|
性染色体異常
|
|
|
|
|
Chromosomes, Fungal
|
真菌染色体
|
|
|
|
|
Polymorphism, Restriction Fragment Length
|
制限酵素断片長多型
|
|
|
|
|
Mutation, Missense
|
ミスセンス変異
|
|
|
|
|
Recombination, Genetic
|
遺伝子組換え
|
|
|
|
|
Codon, Initiator
|
開始コドン
|
|
|
|
|
Base Sequence
|
塩基配列
|
|
|
|
|
Genetic Markers
|
遺伝子マーカー
|
|
|
|
|
Chromosomes, Human, X
|
ヒトX染色体
|
|
|
|
|
Ocular Physiological Phenomena
|
眼生理学
|
|
|
|
|
Heterozygote
|
ヘテロ接合体
|
|
|
|
|
Genes, Recessive
|
劣性遺伝子
|
|
|
|
|
Point Mutation
|
点変異
|
|
|
|
|
Gene Library
|
遺伝子ライブラリー
|
|
|
|
|
Gene Order
|
遺伝子の配列位置
|
|
|
|
|
Exons
|
エクソン
|
|
|
|
|
Gestational Age
|
在胎月齢
|
|
|
|
|
Sequence Deletion
|
配列欠失
|
|
|
|
|
Genetic Variation
|
遺伝的多様性
|
|
|
|
|
Sex Chromosomes
|
性染色体
|
|
|
|
|
Hearing
|
聴覚
|
|
|
|
|
X Chromosome Inactivation
|
-
|
|
|
|
|
Genomic Library
|
ゲノムライブラリー
|
|
|
|
|
Genome, Human
|
ヒトゲノム
|
|
|
|
|
Lod Score
|
ロッドスコア
|
|
|
|
|
Polymorphism, Genetic
|
遺伝子多型
|
|
|
|
|
Dinucleotide Repeats
|
ジヌクレオチド反復
|
|
|
|
|
Genetics, Medical
|
医科遺伝学
|
|
|
|
|
Carrier State
|
保菌者状態
|
|
|
|
|
Mutation
|
変異
|
|
|
|
|
Maternal-Fetal Exchange
|
母体胎児間物質交換
|
|
|
|
|
Protein Structure, Tertiary
|
蛋白質三次構造
|
|
|
|
|
Crossing Over, Genetic
|
遺伝的乗換え
|
|
|
|
|
Birth Weight
|
出生体重
|
|
|
|
|
Cosmids
|
コスミド
|
|
|
|
|
Pregnancy
|
妊娠
|
|
|
|
|
Mutagenesis, Insertional
|
挿入型変異誘発
|
|
|
|
|
Molecular Biology
|
分子生物学
|
|
|
|
|
Centromere
|
セントロメア
|
|
|
|
|
Protein Structure, Secondary
|
蛋白質二次構造
|
|
|
|
|
Introns
|
イントロン
|
|
|
|
|
Homeostasis
|
ホメオスタシス
|
|
|
|
|
Amino Acid Sequence
|
アミノ酸配列
|
|
|
|
|
Phenotype
|
表現型
|
|
|
|
|
Genes
|
遺伝子
|
|
|
|
|
Dosage Compensation, Genetic
|
遺伝子量補正
|
|
|
|
|
Polymorphism, Single-Stranded Conformational
|
PCR-SSCP法
|
|
|
|
|
Sequence Homology, Amino Acid
|
アミノ酸配列相同性
|
|
|
|
|
Visual Fields
|
視野
|
|
|
|
|
Organ Specificity
|
臓器特異性
|
|
|
|
|
Codon, Nonsense
|
ナンセンスコドン
|
|
|
|
|
Probability
|
確率
|
|
|
|
|
Visual Acuity
|
視力
|
|
|
|
|
Repetitive Sequences, Nucleic Acid
|
核酸反復配列
|
|
|
|
|
Alleles
|
対立遺伝子
|
|
|
|
|
Nucleic Acid Hybridization
|
核酸ハイブリダイゼーション
|
|
|
|
|
Promoter Regions, Genetic
|
プロモーター領域
|
|
|
|
|
Translocation, Genetic
|
転座
|
|
|
|
|
Risk Factors
|
危険因子
|
|
|
|
|
Transfection
|
トランスフェクション
|
|
|
|
|
Gene Expression Regulation
|
遺伝子発現調節
|
|
|
|
|
Gene Deletion
|
遺伝子欠失
|
|
|
|
|
Genotype
|
遺伝子型
|
|
|
|
|
Haplotypes
|
ハプロタイプ
|
|
|
|
|
Incidence
|
発生率
|
|
|
|
|
Genetic Testing
|
遺伝学的スクリーニング
|
|
|
|
|
Chromosome Aberrations
|
染色体異常
|
|
|
|
|
Gene Frequency
|
遺伝子頻度
|
|
|
