hereditary disease

用法例句

Polyalanine expansion in human genetic diseases;

多聚丙氨酸延展突变与人类遗传病

Dynamic Mutation-A new mutation type leading tohuman genetic diseases;

动态突变——人类遗传病发生的一种新机制

According to the different position in chromosome and dominance and recessiveness of a disease,hereditary diseases can be classified in four categories: autosomal dominant inherited disease,autosomal recessive inherited disease,sex chromosome dominant inherited disease and sex chromosome recessive inherited disease.

遗传病是指生殖细胞或受精卵内的遗传物质产生改变而引起疾病。

The paper expounds the types and characteristics of hereditary disease and analyzes the relations between the heredities of x chromosome and common chromosome according to the inheritance spectrum.

阐述常见遗传病的种类和特点,及根据遗传图谱分析X染色体遗传和常染色体、遗传的关系。

The hereditary disease convert into the one of main reason to harming health of mankind, The study of biology had clarified a lot of occurring mechanism of hereditary disease; Had drawn atlases of human gene forms, had launched the seeking of gene diagnosis and gene treats, had set medical science to soar, It must be raise the level of.

遗传病成为当今危害人类健康的主要原因之一 ,生物学的研究已阐明许多遗传病 (包括癌症 )发生的机理 ,绘制了人类基因组图谱 ,开展了基因诊断和基因治疗的探索 ,推动医学腾飞 ,必将空前提高人类健康水

Application of fluorescence in situ hybridization in the diagnosis of genetic diseases;

荧光原位杂交技术在遗传病诊断中的应用

Genetic counseling is an important means of precaution against the birth of babies with genetic diseases, of decreasing the incidence of genetic diseases and of promoting people s innate qualities.

遗传咨询是预防遗传病患儿出生、降低遗传病发病率、提高人口先天素质的重要手段。

Design and realization of the network medical system for genetic disease based on Internet;

基于Internet的遗传疾病登记、随访系统的设计与实现

The development of genetic technology makes it possible for human beings to control genetic diseases by intervening the reproductive process.

基因技术的发展使人们通过干预生殖过程来控制遗传疾病变得可能。

The mechanisms of human genetic diseases and strategies to test human genetic diseases are discussed in the review.

论述了遗传性疾病的发病机理和遗传病诊断的途径和策略,着重介绍了人类遗传疾病基因诊断技术的原理和发展状况,对该领域的新成果作了介绍和总结,对发展动向和存在的问题作了简要论述。

The Basis and Method for Judgement on the Different Modes of Inheritance of Hereditary Diseases;

关于遗传病不同遗传方式的判断依据与方法

a hereditary disorder of lipid metabolism occuring most frequently in individuals of E European Jewish descent; accumulation of lipids in nervous tissue results in death in early childhood.

一种脂变态的遗传病，多出现在欧洲。

a disorder of lipid metabolism that is inherited as an autosomal recessive trait.

油脂新陈代谢混乱的一种遗传病症。

hereditary metabolic diseases of nervous system

神经系统遗传代谢病

hereditary hypophosphatemic rickets

遗传性低磷酸佝偻病

genetic and congenital disorder

遗传性与先天性疾病

Analysis of Genetic Epidemiology and Genetic Model of Psoriasis Vulgaris;

寻常型银屑病遗传流行病学及遗传模式分析

Molecular Genetics of Pathogenesis of Congenital Nephrogenic Diabetes Insipidus;

遗传性尿崩症发病机理的分子遗传学研究

Cytogenetics and Epigenetics of Acute Leukemia

急性白血病的细胞遗传学及表观遗传学研究

Gene Mutations in Psoriasis and Marie Unna Hereditary Hypotrichosis

银屑病及Marie Unna遗传性稀毛症的遗传易感基因

Genetic Analysis of Special Corn Inbredlines to S.reilianum and Genetic Diversity of S.reilianum;

特用玉米抗丝黑穗病遗传分析及其病菌致病性的遗传多样性

Pathogenicity and Genetic Diversity of Rice Stripe Virus;

水稻条纹病毒致病性及其遗传多样性

Reverse Genetics System of Rabies Virus CTN Strain

狂犬病病毒CTN株反向遗传系统的建立

Clinic analysis of hereditary gingival fibromatosis

遗传性牙龈纤维瘤病的临床病例分析

Molecular and Clinical Pathology Features of Hereditary Non-Polyposis Colorectal Cancer (HNPCC);

遗传性非息肉病性结直肠癌的分子遗传及临床病理研究

Genetic Analysis of Resistant Genes to Rust and Powdery Midew and Brown Spot in Adzuki Bean

小豆锈病、白粉病及褐斑病的抗性基因遗传分析

hereditary hypophosphatemia rickets

遗传性低磷酸盐性佝偻病

Nowadays the pathogenesis of CFEOM has been studied in clinical pathology and molecular genetics fields, and researchers have found that it is a kind of primary neuropathy with secondary myopathic changes and that it has 3 genetic loci and 1 disease gene.

并发现3个遗传位点和1个致病基因。