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- The recurrence risk for this disease is, of course, 25% because of the autosomal recessive inheritance pattern. 因为它是常染色体隐性遗传的，所以它在家族中的发病率是25%25。
- The frequencies of non Mongolia wrinkle were 15.41% and 5.42%,the frequencies of autosomal recessive inheritance were 0.3925 and 0.2328 respectively. 蒙古褶为无的出现率分别为15.;41%25和5
- Keywords hearing impairment;autosome recessive inheritance;SLC26A4 gene;denaturing high performance liquid chromatography （DHPLC）;mutation;molecular epidemiology; 耳聋;常染色体隐性遗传;SLC26A4基因;变性高效液相色谱（DHPLC）;基因突变;分子流行病学;
- autosomal recessive inheritance(AR) 常染色体隐性遗传
- autosome recessive inheritance 常染色体隐性遗传
- Objective:To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes. 目的:探讨常染色体隐性遗传性共济失调家系的临床特征并排除已知的致病基因。
- Complex vertebral malformation (CVM), a lethal autosomal recessive inherited defect in Holstein breed, was newly reported in Demark. 摘要荷斯坦奶牛脊柱畸形综合征是近年新发现的一种常染色体隐性遗传病，该病对纯合子胎儿是致死性的。
- autosomal recessive inherited disease 常染色体隐性遗传病
- The Proportion and Clinical Feature of Duchenne Muscular Dystrophy With Autosomal Recessive Inheritance 常染色体隐性遗传的类Duchenne肌营养不良临床特征及其发生比率的估计值分析
- autosomal recessive inheritance 常染色体隐性遗传
- It can be autosomal dominant, autosomal recessive, or X-linked mode of inheritance. 他可以是体染色体显性、体染色体隐性、或是性联遗传等方式的遗传疾病。
- Two congenital deaf and dumb pedigrees were reported,the hereditary model of two congenital deaf and dumb pedigree was autosome recessive heredity,which controlled by two pairs of genes. 报道了两个先天性聋哑家系.;这两个家系中的先天性聋哑属常染色体隐性遗传，且有两对基因控制。
- Abstract： Two congenital deaf and dumb pedigrees were reported,the hereditary model of two congenital deaf and dumb pedigree was autosome recessive heredity,which controlled by two pairs of genes. 摘 要： 报道了两个先天性聋哑家系.;这两个家系中的先天性聋哑属常染色体隐性遗传，且有两对基因控制。
- Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance. 先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。
- Xeroderma pigmentosum is an autosomal recessive disease. 着色性干皮病是一种常染色体的退行性疾病。
- Polygenic inheritance can sometimes mimic either dominant or recessive inheritance, and this feature may lead to erroneous conclusions regarding the type of underlying genetic abnormality. 多基因遗传疾病通常在显性遗传和隐性遗传中又是极其相似的，这些原因会误导对于基因类遗传疾病种类的判断.
- 5. Complex vertebral malformation (CVM), a lethal autosomal recessive inherited defect in Holstein breed, was newly reported in Demark. 多指（或趾）畸形的人（或动物）有超过正常数目足趾或手指的人或动物收藏指正
- BackgroundHereditary spastic paraplegia (HSP or SPG) is a kind of hereditary disorder of nervous system. Autosomal dominant (AD), autosomal recessive (AR), X-linked inheritance have been described for HSP. 遗传性痉挛性截瘫(hereditary spastic paraplegia，HSP或SPG)是一种神经系统遗传病，呈常染色体显性遗传(autosomal dominant，AD)、常染色体隐性遗传(autosomal recessive，AR)和X-连锁隐性遗传(X-linked recessive，XR)，其中以AD遗传最为常见。
- The mode of inheritance of our cases is thought to be autosomal recessive according to their family history: Because of no subretinal neovascular membrane noted laser treatment is not neceesary. 本病例由家族史看来可能为自体隐性遗传，萤光眼底摄影显示无网膜下新生血管，故未予雷射治疗。
- sex-linked recessive inheritance 性连锁隐性遗传
