索引
A
| α-fetoprotein |
甲胎蛋白 |
133 |
| α-thalassemia |
甲型地中海贫血 |
64 |
| abnormal hemoglobin |
异常血红蛋白 |
61 |
| ABO blood group |
ABO血型 |
50 |
| acetyl-transferase |
乙酰化酶 |
11 |
| acetylcholine esterase |
乙酰胆碱酯酶 |
133 |
| achromatopsia |
全色盲 |
53 |
| additive effect |
累积效应 |
83 |
| addittive gene |
累加基因 |
83 |
| adenine |
腺嘌呤 |
34 |
| adenosine deaminase |
腺苷脱氨酶 |
46 |
| adenovirus-polylysine DNA-complex |
腺病毒多赖氨酸DNA复合体 |
169 |
| adult polycystic kidney diseade(APKD) |
成人多囊肾病 |
166 |
| affinity banding agent |
亲和结合剂 |
143 |
| agammaglobinemia |
无丙球蛋白血症 |
67 |
| albinism |
白化病 |
52，77 |
| alcohol dehydrogenase |
乙醇脱氢酶 |
115 |
| aldehyde dehydrogenase |
乙醛脱氢酶 |
115 |
| allele specific oligonucleotide |
等位特异性寡核苷酸 |
162 |
| α-globin gene cluster |
α珠蛋白基因簇 |
60 |
| allopurinol |
别嘌呤醇 |
143 |
| alpecia,hereditary |
遗传性早秃 |
55 |
| alpha-thalassemia |
α地中海贫血 |
64，164 |
| Alu family Alu |
家族 |
41 |
| amniocentasis |
羊膜穿刺 |
131 |
| Amp-FLP |
扩增片段长度多态性 |
162 |
| amplification |
扩增 |
161 |
| amplified fragment length polymorphism |
扩增片段长度多态性 |
162 |
| anaphase lag |
后期迟留 |
14 |
| ankyrin |
锚蛋白 |
70 |
| aneuploidy |
非整倍性，异倍性 |
13 |
| angiotensin converting enzting enzyme |
血管紧张素转化酶 |
|
| angiotensinⅡ |
血管紧张素Ⅱ |
87 |
| angiotensinogen |
血管紧张素原 |
87 |
| antenatal diagnosis |
出生前诊断 |
130 |
| antihemophilic globulin |
抗血友病球蛋白 |
72 |
| antioncogene |
抗癌基因 |
125 |
| antiparallel |
反向平行排列 |
14 |
| antisense strand |
反义链 |
36 |
| antisense oligdeoxynucleotide |
反义寡核苷酸 |
167 |
| antisense technology |
反义技术 |
167 |
| antithrombin Ⅲ deficiency |
抗凝血酶Ⅲ缺乏症 |
73 |
| α-antitrypsin |
α-抗胰蛋白酶 |
116 |
| arch |
弓形纹 |
134 |
| arch,tented loop |
蓬账弓形纹 |
134 |
| arylhdrocarbon hydroxylase |
芳烃羟化酶 |
116，120 |
| ASO |
等位特异性寡核苷酸 |
162，165 |
| association |
关联 |
6 |
| ataxia telangiectasia,AT |
毛细血管扩张性共济显性遗传 |
119 |
| autosomal dominance inheritance |
常染色体显性遗传 |
49 |
| recessive inheritance |
常染色体显性遗传 |
52 |
| axial triradius |
轴三叉 |
135 |
| 5′-azocytidine |
5氮胞苷 |
167 |
B
| balanced franslocation |
平衡易位 |
16 |
| Barts hydrops fetalis Barts |
水肿胎， Barts胎尔水肿综合征 |
64 |
| basal cell nevus syndrome |
基底细胞痣 |
118 |
| Becker′s muscular dystrophy |
轻型假肥大型肌营养不良 |
71 |
| β-globin gene cluste |
β珠蛋白因簇 |
60 |
| β-thalassemia |
β地中海贫血 |
65 |
| Bloom′s syndrome Bloom′s |
综合征 |
19，119 |
| blunt terminus |
平整末端 |
157 |
| brachydactyly |
短指症 |
49，86 |
| break point cluster region |
断点簇区 |
122 |
| breakage |
断裂 |
14 |
| brnachitis,chronic |
慢性支气管炎 |
115 |
| bronchial asthma |
支气管哮喘 |
115 |
| Burkitt lymphoma |
非洲恶性淋巴瘤 |
122 |
C
| 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 |
| , 百拇医药 |