CAAT box CAAT | 框(盒) | 32 |
calitonin | 降钙素 | 39 |
calcitonin gene related pepitde | 降钙素基因相关肽 | 39 |
cancer genetics | 肿瘤遗传学 | 2,117 |
cancer family | 癌家族 | 117 |
candidate gene approach | 侯选基因方法 | 109 |
carcinogenesis | 致癌 | 1 |
caucinoma,familial | 家族性癌 | 117 |
carrier,genetic | 遗传携带者 | 52,139 |
obligatory | 肯定携带者 | 52 |
probable | 可能携带者 | 52 |
cDNA probe | 探针 | 155 |
cell fusion | 细胞融合 | 104 |
character | 着丝粒融合 | 16 |
chimetic minigene | 性状 | 1 |
cholestyamine | 嵌合小基因 | 173 |
chorionic villi aspiration sampling | 消但胺 | 143 |
chromosomal disease | 绒毛取样 | 132 |
assignment | 染色体病 | 9,10,20 |
aberration | 染色体定位 | 130 |
loss | 染色体畸变 | 20,43 |
chronic bronchitis | 染色体丢失 | 14 |
obstractive pulmonary disease | 慢性支气管炎 | 115 |
clastogen | 慢性阻塞性肺疾患 | 115 |
cliical genetics | 断裂剂 | 14,138 |
clone panel method | 临床遗传学 | 1 |
clnidene | 克隆嵌板法 | 105 |
coding strand | 可乐定 | 30 |
co-dominance | 编码链 | 36 |
codon deletion | 共显性 | 50 |
codon insertion | 整码缺失 | 45 |
cohesive termius | 密码子插入 | 45 |
complemetn deficiency | 粘性末端 | 157 |
complete androgen insensitivity syndrome | 补体缺乏症 | 69 |
complete dominance | 雄性素全不敏感综合征 | 75 |
complex genetic disease | 完全显性 | 49 |
componet analysis | 复杂性遗传病 | 84 |
concordance | 疾病组分分析 | 6 |
condensation | 一致率,同病率 | 5 |
conditional probability | 凝缩,固缩 | 10 |
congenital | 条件概率 | 147 |
pancytopenia | 先天性 | |
disease | 先天性全血细胞减少症 | 119 |
anomaly | 先天性疾病 | 8 |
anomaly | 先天畸形 | 8 |
absence of one kidney | 先天性单测肾缺如 | 86 |
deficiency of activated protein C inhibitor | 先天性活化蛋白C抑制物缺乏症 | 74 |
heart defect | 先天性心脏缺陷 | 86 |
malformation | 先天畸形 | 84 |
consanguineous marrige | 近亲婚配 | 96 |
consensus sequence | 一致顺序 | 32 |
cordocentasis | 脐血抽吸 | 132 |
coronary artery diseace | 冠心病 | 87 |
counselee | 咨询者 | 145 |
counseling,genetic | 遗传咨询 | 145 |
counselor | 咨询医生 | 145 |
criss-cross inheritance | 交叉遗传 | 53 |
cryptic splicing site | 隐蔽裂解位点 | 69 |
cystic fibrosis | 囊性纤维化 | 59 |
cytogenetic map | 细胞遗传图 | 103 |
cytogenetics | 细胞遗传学 | 1 |
cytosine deaminase | 胞嘧啶脱氨酶 | 172 |
cytosine | 胞嘧啶 | 34 |