1)nonsyndromic inherited hearing loss非综合征型遗传性耳聋
2)non-syndromic hearing loss遗传性非综合征型耳聋
英文短句/例句
1.Association Studies on Susceptibility Loci (Gene) of Two Types of Non-syndromic Hearing Impairment;遗传性非综合征型耳聋两种致病基因易感位点的关联分析
2.Optimization and Application of Genetic Diagnostic System for Hereditary Nonsyndromic Hearing Loss遗传性非综合征型耳聋基因诊断体系的优化和应用
3.Molecular Genetic Analysis of Waardenburg Syndrome and Non-syndromic Hearing LossWaardenburg综合征和非综合征型耳聋的分子遗传学研究
4.Genetic Analysis of Non-syndromic Hearing Loss and Waardenburg Syndrome;非综合征性耳聋及Waardenburg综合征的遗传学分析
5.Molecular Finding in Two Chinese Families with Nonsyndromic Hearing Impairment;两个非综合征型耳聋家系的分子遗传学研究
6.Mapping and Identified the Causative Genes in Chinese Nonsyndromic X-linked Hereditary Hearing Loss Pedigrees;非综合征型X连锁显性遗传耳聋家系致病基因的定位及鉴定研究
7.Alport's syndrome遗传性肾炎神经性耳聋综合征;阿尔波特氏综合
8.Mutation Analysis of GJB3 in HAN PEOPLE with Non-syndromic Hearing Impairment in Xinjiang新疆地区汉族遗传非综合征型耳聋人群GJB3基因突变分析
9.The Study of the Deafness Gene GJB2 Mutation in a Hereditary Nonsyndromic Deaf Families;遗传性非综合征性耳聋一家系人群GJB2基因突变的研究
10.Mutation analysis of GJB3 between Chinese and Uighur population with nonsyndromic hearing impairmentGJB3基因在新疆维汉两民族遗传性非综合征耳聋患者的突变分析
11.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
12.Molecular Mechanism of Late-onset Nonsyndromic Hearing Loss and Age-related, Aminoglycoside-induced Hearing Loss迟发性非综合征型耳聋及老年性、药物性耳聋的分子机制研究
13.Molecular Mechanism and Functional Characterization Associate with Maternally Inherited Aminoglycoside-induced and Nonsyndromic Deafness;母系遗传药物性聋与非综合征性聋的分子遗传机制与功能研究
14.Clinical character and etiological study of a large family with maternally inherited non-syndromic deafness一母系遗传非综合征耳聋大家系的临床特征和病因学研究
15.Study on the Mitochondrial DNA Mutation and the Phenotype Diversity of Nonsyndromic Hearing Loss;非综合征型耳聋线粒体DNA突变及其临床表型多样性的研究
16.Molecular Genetic Analysis of the Mitochondrial DNA 1555 Mutation Gene among Nonsyndromic Hearing Impairment Patients from Jilin Province;吉林省非综合征型耳聋分子病因学分析
17.Mutation analysis of GJB2 gene in deaf population from Chongqing city重庆市非综合征型耳聋患儿GJB2基因突变分析
18.Molecular genetic analysis of the mtDNA A1555G mutation in patients with non-syndromic hearing loss非综合征型耳聋线粒体基因A1555G突变分析
相关短句/例句
non-syndromic hearing loss遗传性非综合征型耳聋
3)nonsyndromic/syndromic非综合征型遗传性耳聋/综合征型遗传性耳聋
4)hereditary nonsyndromic deafness遗传性非综合征性耳聋
5)autosomal-dominant non-syndrome deafness常染色体显性遗传非综合征型耳聋
1.Mapping of gene underlying autosomal-dominant non-syndrome deafness;常染色体显性遗传非综合征型耳聋致病基因的定位研究
6)NSHL遗传性非综合性耳聋
延伸阅读
不完全性遗传性男性假两性畸形综合征Ⅰ型不完全性遗传性男性假两性畸形综合征Ⅰ型 病名。亦称雄激素抵抗综合征Ⅰ型。系X伴性遗传。性腺正常，精子产生不足。中肾管发育程度不一，中肾管衍生器官缺如。临床症状包括各种亚综合征(以前认为是独立疾病)：从表现为女性的Lub综合征到GilberDreyfus综合征和Reifenstein综合征，直到至均不呈男性表现型的Rosewaters综合征。每种亚综合征各有其有关的心理问题和对调整性别的不同需要。体征从具有假阴道的女性表现型(Lub综合征)到正常不育男性(尿道下裂常见)，体毛正常，胡须稀少或缺如。染色体研究示男性性染色体46XY核型。血液的睾酮生成正常或增高，雌激素生成高于正常男子，促性腺激素水平增高。治疗因各种亚综合征而异。对睾酮的雄激素同化作用有抵抗性。预后良好。不影响寿命。
