1.
a disease caused by a dominant mutant gene on an autosome.
由于常染色体突变基因导致的疾
2.
Chromosome mutation A change in the number or arrangement of genes in a chromosome.
染色体突变：生物细胞中染色体数目的增减和结构的改变。
3.
The addition, as by mutation, of one or more nucleotides to a chromosome.
染色体突增由于突变而使染色体增加一个或多个核苷酸
4.
Paternity Index Calculation in Mutation Autosomal STR Locus
常染色体STR突变基因座父权指数计算
5.
a disease caused by the presence of two recessive mutant genes on an autosome.
由于常染色体上出现突变基因而导致的疾
6.
The Study on the Principle of Enterprise Reengineering--“Enterprise Chromosome”Mutation Model
企业再造机理研究——企业“染色体”突变模型
7.
Chromosome Location and Regional Assignment of the Human Lung Cancer-associated Gene Related with PP2Ac Pointmutation by the Chromosome Fluorescence in Situ Hybridization;
PP2Ac突变型肺癌相关基因在染色体区域的定位
8.
Analysis of the mutations of rhodopsin gene in autosomal dominant retinitis pigmentosa family
常染色体显性遗传视网膜色素变性家系视紫红质基因突变分析
9.
environmental pollution and chromosomal aberration
环境污染与染色体畸变
10.
Two New Scant Hair Mice Induced by ENU and Mapping of the Mutant Gene on Chromosome;
ENU诱变获得两例新的稀毛小鼠及其突变基因的染色体定位
11.
Comparative Study on Human Peripheral Blood Chromosome Aberration,Micronucleus and HPRT Gene Mutation Induced by Neutron Irradiation
中子辐射诱发人外周血染色体畸变、微核HPRT基因突变的比较研究
12.
Study on Targeted Correction of Point Mutation in Low Density Lipoprotein Receptor Gene in Situ of Chromosome and Regulatable Expression;
低密度脂蛋白受体基因点突变染色体原位修复及调控表达的研究
13.
Missense mutation in the βB1-crystallin gene caused autosomal dominant congenital cataract in China
晶状体蛋白βB1基因错义突变引起常染色体显性遗传性白内障
14.
Mutation Analysis of Retinitis Pigmentosa I Gene in Chinese Patients with Autosomal Dominant Retinitis Pigmentosa
常染色体显性遗传视网膜色素变性家系视网膜色素变性1基因（RP1）的突变分析
15.
an organism that has characteristics resulting from chromosomal alteration.
染色体变异的生物体。
16.
Gene Localization and a Novel Mutation Identified for Non-syndromic Hearing Loss;
常染色体显性遗传非综合症型耳聋基因的定位与突变筛查
17.
Preliminary Study on Palindromic Sequence-mediated De Novo Chromosomal Mutations in Human Sperms;
回文序列介导的人类精子中染色体新突变发生规律初探
18.
MAPPING OF THE MUTANT GENE OF KUNMING SPARSE MOUSE AND STUDYING ITS PATHOLOGY;
昆明稀毛小鼠突变基因的染色体定位及病理研究