1.
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
2.
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。
3.
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
4.
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。
5.
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
6.
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
7.
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
8.
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。
9.
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
10.
Linkage Mapping of the Two Chinese Family with Autosomal Dominant Retinitis Pigmentosa;
两个常染色体显性遗传视网膜色素变性家系连锁分析
11.
FHCM is a heterozygote autosomal dominant disease, and the incidence rate in male is obvious higher than that in female.
属杂合子常染色体显性遗传性疾病,男性患病率高于女性。
12.
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
13.
Neurofibromatosis is one of autosomal-dominant neurogenetic diseases with relatively low incidence.
神经纤维瘤病是一常染色体显性遗传性疾病，临床上较为少见。
14.
This is tuberous sclerosis, an autosomal dominant condition characterized by mental retardation and seizures beginning early in life.
结节性硬化症，常染色体显性遗传，表现为智力低下、癫痫发作等。
15.
The Study of Causative Genes in a Chinese Family with Autosomal Dominant Congenital Cataract;
常染色体显性遗传先天性白内障一家系致病基因研究
16.
Studies on the Clinical Classification and Treatment of Highly Symptomatic Adult Polycystic Liver Disease;
常染色体显性遗传性多囊肝病临床分期和治疗方式选择的研究
17.
Clinical, Pathological and Molecular Biological Study on Autosomal Dominant Inherited Centronuclear Myopathy;
常染色体显性遗传性中央核肌病一家系临床、病理和基因研究
18.
Candidate Gene Screening for Autosomal Dominant Auditory Neuropathy in a Chinese Pedigree;
常染色体显性遗传性听神经病家系候选基因突变筛查