1.
Progress in the gene-related study on autosomal retinitis pigmentosa
常染色体遗传型视网膜色素变性相关基因的研究进展
2.
sex-limited autosomal dominant inheritance
性限常染色体显性遗传;限性常染色体显性遗传
3.
According to genetic analysis, this disease is caused by autosomal dominant inheritance.
经过遗传分析，认为该畸形属常染色体显性遗传。
4.
Cytogenetical analysis on 218 cases with chromosomal abnormality
218例染色体异常者的细胞遗传学分析
5.
With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance.
据系谱分析,该疾病符合常染色体显性遗传方式。
6.
Molecular Cytogenetic Detection of Minute Chromosomal Structural Abnormality on the Chromosomal Terminal Regions
染色体末端微小结构异常的分子细胞遗传检测
7.
The Study of Disease-Causing Genes of Autosomal Dominant Congenital Cataract;
常染色体显性遗传白内障致病基因的研究
8.
Laparoscopic Management of Autosomal Dominant Polycystic Kidney;
常染色体显性遗传性多囊肾病的腹腔镜治疗
9.
Preimplantation Genetic Diagnosis for Patients with Chromosome Structure Abnormalities;
染色体异常者的胚胎植入前遗传学诊断研究
10.
Human Population Genetic Structures Revealed by High Density Autosomal SNPs;
高密度常染色体SNPs揭示的现代人群遗传结构
11.
Application of autosomal STR genetic markers in siblings identification;
常染色体STR遗传标记在同胞鉴定中的应用
12.
Cytogenetic analysis on 1247 abnormal chromosome patients
1247例染色体异常患者的细胞遗传学分析
13.
Cytogenectical Analysis of 128 Cases abnormal karyotype
128例异常染色体核型的细胞遗传学分析
14.
Progress in treatment of autosomal dominant polycystic kidney disease
常染色体显性遗传多囊肾病的治疗研究进展
15.
The Genetic Polymorphism and the Structural Analysis of STR Loci of Miao Nationality in Yunnan Province
云南苗族常染色体STR遗传多态性及其遗传结构分析
16.
Clinical genetics and gene mapping studies on a family with autosomal dominant congenital cataract
常染色体显性遗传性白内障一家系的临床遗传学及基因定位研究
17.
HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
HHT是常染色体显性遗传性血管发育异常的一种疾病。
18.
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