A study of DJ-1 gene in 3 pedigrees with autosomal recessive early-onset Parkinson s disease;
常染色体隐性遗传早发型帕金森病家系的DJ-1基因研究
Clinical features of autosomal recessive juvenile Parkinson disease;
常染色体隐性遗传性青少年型帕金森病的临床特征
Papillon-Lefèvre syndrome(PLS) is an extremely rare inherited disease as an autosomal recessive trait.
掌跖角化-牙周破坏综合征(PLS)是一种罕见的常染色体隐性遗传性疾病,其特点是手掌和脚掌部位的皮肤过度角化以及乳、恒牙过早脱落。
High-resolution Ultrasonography in the Assessment of Autosomal Recessive Polycystic Kidney Disease
高分辨超声在常染色体隐性遗传性多囊肾诊断中的价值
A Novel Gene is a Positional Candidate for Autosomal Recessive Polycystic Kidney Disease(ARPKD);
常染色体隐性遗传性多囊肾相关新基因的克隆及其特征
Consider as what recessive heredity causes euchromosome to high myopia.
对于高度近视则认为是常染色体隐性遗传引起的。
Analysis of the Relatoin between Gene Mutation and Clinical Phenotype for Autosomal Recessive Families
常染色体隐性遗传耳聋家系基因突变与临床表型的研究
It is a recessive hereditary disease of autosome to be deaf and dumb. It was analysed through heredity that reducing or preventing consanguineous marriage can reduce the deaf-mute's birth rate.
聋哑是常染色体隐性遗传病,通过遗传分析发现,减少或防止近亲结婚可以降低聋哑人的出生.
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
Twisting tongue is the recessive heredity of single gene of autosome, while the positive type is the recessive character.
翻舌为常染色体单基因隐性遗传,阳性为隐性性状。
The inheritance pattern of EDMD includes X-linked recessive, autosomal dominant and recessive modes.
其遗传方式为X-连锁隐性、染色体显性和隐性遗传。
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。
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
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
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。
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
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
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
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。
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
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