目的研究原发性高血压家族性的遗传方式。
Objective To investigate the familial genetic model of essential hypertension (EH).
蒙古羊胸椎数的遗传方式具有亲本印记特征。
Multi-vertebral characters of Mongolia sheep has a feature of parental imprinting.
目的探讨脊肌萎缩症的临床特点和遗传方式。
Objectives To investigate the clinical features and the onset pattern of spinal muscular atrophy.
该策略的前提条件是与抗性遗传方式密切相关。
The supposition of this strategy ties up the inheritance mode of resistance.
最近对线粒体和非传统的遗传方式已有所了解。
More recently, mitochondrial and nontraditional patterns of inheritance have been recognized.
目的为了探讨特发性癫痫(iep)的遗传方式。
Objective To explore genetic patterns of idiopathic epilepsy (IEP).
目的：确定该家系遗传病的临床类型和遗传方式。
Objectve: To determine the clinical type and inheritance mode of congenital anodontia.
目的探讨瓣状甲的类型、性别和年龄分布及其遗传方式。
Objective: To research the types, the distributions for gender and age, and the hereditary mode of the petaloid toenails.
第二，应用分离分析法确定内蒙古绒山羊胎产羔数的遗传方式。
Second, the segregation analysis was applied to determine inheritance mode of litter size in Inner Mongolian cashmere goat.
目的探讨遗传因素在普通型偏头痛发生中的作用及该病的遗传方式。
Purpose to research roles of genetic factors on occurrence of migraine without aura and hereditary modes of the disorder.
遗传病遗传方式的判断是高中《生物》教材的一个重点、难点问题。
How to judge the way of heredity on illness caused by heredity is an important and difficult problem in Senior Biology textbook.
本文综述了线粒体病的特点，并对线粒体病的母系遗传方式进行了分析。
This review summarized some characteristics of mitochondrial diseases, and analysed the pattern of maternal inheritance about mitochondrial diseases.
本文对ABO血型的抗原物质形成过程、遗传方式和实践应用作了阐述。
This thesis makes a systematic exposition of antigen of ABO blood type: its process of taking shape, inheritance and its application.
作者对这个家系进行了回顾性研究，以期探讨该病的遗传方式、特点及鉴别诊断。
A retrospective study was done of this genealogy to discuss the genetic form and characteristics, and the differential diagnosis.
突变的TH受体对功能正常的TH受体的功能的限制是因为占主要优势的遗传方式。
Interference with the function of the normal TH receptor by mutant TH receptors is responsible for the dominant mode of inheritance.
方法：采用分离分析方法和多基因阈值理论对75例惊恐障碍家系进行遗传方式探讨。
Method: 75 genealogy with panic disorder were studied by segregation analysis and polygene threshold theory.
目的应用分子生物学方法判定经家系分析初步认定为X连锁遗传的高度近视家系的遗传方式。
Objective Using molecular biological method to determine the inherited modal of a family which was considered as X-linked high myopia by pedigree analysis.
这是一种癌症的间接遗传方式，即这种遗传病在将来50%成为癌症，所以说癌症是可以遗传的。
This is the indirect and genetic pattern of a kind of cancer, namely this kind of hereditary disease is in in the future 50% become cancer, say cancer is OK so genetic.
目的：报告及分析高发癌家系的遗传方式，探讨癌家族肿瘤发生与遗传、环境及饮食习惯之间的关系。
Objective: to know the hereditary pattern of a pedigree with multi-cancer history and to explore the relationship between pathogenesis and heredity, environment and dietary pattern in cancer family.
Law博士和Constantino博士称，他们的发现为深入研究自闭症及其相关症状的遗传方式提供了思路。
Law and Constantino say their findings provide insight into the inheritance patterns of autism and its associated traits.
前言：目的：研究人类手掌小鱼际区真实花纹的家系特点，了解人类手掌小鱼际区真实花纹的遗传方式。
Objective: To study the pedigree character of the true pattern in palmar hypothenar area, and study the genetics of the true pattern in human palmar hypothenar area.
目前研究发现此病有三种遗传方式：即母源第7号染色体单亲双体、常染色体显性遗传及常染色体隐性遗传。
At present, three modes of inheritance are identified including maternal uniparental disomy for chromosome 7 and autosomal dominant or autosomal recessive inheritance.
目的：探索家族性2型糖尿病的遗传方式及家族性2型糖尿病家系一级亲属正常糖耐量同胞的血糖血脂代谢变化。
Objective:To investigate the inheritance mode of familial type 2 diabetes and to study the changes of blood glucose and lipid levels in normal siblings.
T1和T2代中潮霉素抗性表现为显性单基因位点的遗传方式，符合孟德尔分离规律，并得到分子鉴定结果的证实。
Mendelian inheritance of hygromycin resistance was showed as single dominant locus and proved by Southern blotting analysis in T1 and T2 generation of all transgenic plants.
目前根据遗传方式分为1型（常染色体显性）和2型（常染色体隐性） ，每一型根据不同基因缺陷又分为许多亚型。
The limb-girdle muscular dystrophies are divided into two types according to inheritance pattern, type 1 is autosomal dominant and type 2 is autosomal recessive.
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。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
结果：主要影响样本大小的参数为易感基因频率、环境因素暴露率、基因遗传方式，而疾病的发生率对样本量影响很小。
Results: The most influential parameters of sample size were susceptibility frequency of the genotype, environmental exposure factors in the population, and genetic modes.
结果：主要影响样本大小的参数为易感基因频率、环境因素暴露率、基因遗传方式，而疾病的发生率对样本量影响很小。
Results: The most influential parameters of sample size were susceptibility frequency of the genotype, environmental exposure factors in the population, and genetic modes.
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