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 |