pedigree analysis的例句大全

In this basic, performance test, evaluation of breeding value, computation of maternal and terminal index and pedigree analysis have been carried out.

在此基础上对基础群的个体开展了性能测定，进而进行了育种值的估计、父系或母系指数的计算以及系谱分析，实现了基础群的选种、选配。

Gene diagnosis and pedigree analysis in families of Duchenne and Becker muscular dystrophy

进行性肌营养不良症基因诊断及家系分析

Clinical characteristics and pedigree analysis of a familial isolated atrial septal defect

家族性单纯房间隔缺损的临床特点和系谱分析

Dyskeratosis congenita: a case report and the family pedigree analysis

先天性角化不良1例及家系调查

The Current Situation and the Pedigree Analysis of South China Tiger

华南虎现状及谱系分析

Pedigree analysis of T53 → C in intron 1 and C59 → A in intron 4 mutations of apolipoprotein M gene expression

载脂蛋白M基因1号内含子T53→C和4号内含子C59→A突变的家系分析

Conclusion: Pedigree analysis show a vague rule of inheritance. Further study should be done to find out the relation between NVM and HCM.

结论：通过家系调查提示心肌致密化不全心肌病有遗传性，但遗传规律尚不能明确，且本研究首次发现该病与肥厚型心肌病同时出现在一个家系中，其联系有待进一步研究。

Pedigree analysis of the double heterozygote of hemoglobin G disease combined with alpha thalassemia 2

血红蛋白G病复合α地中海贫血2的家系分析

The function and menu structure of the computer program package of the population and pedigree analysis of human and medical genetics designed by C language are described briefly in this paper.

本文介绍我们用C语言编制的人类与医学遗传学群体与家系资料分析计算机系统的菜单结构与各子系统的功能。

clinical features and pedigree analysis of chinese infantile convulsions with paroxysmal choreoathetosis

中国人婴儿惊厥伴发作性手足舞蹈徐动征临床特征分析

a pedigree analysis of a family with familial hypercholesterolemia

家族性高胆固醇血症一家系分析

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.

Pedigree analysis suggests that FASD is a autosome dominant heredity disease.

家谱分析显示，遗传方式符合常染色体显性遗传。

Familial atrophia maculosa varioliformis cutis: Case report and pedigree analysis

皮肤痘疮样斑状萎缩：病例报道及家系调查

Three Homozygous Patients of Familial Hypercholesterolemia Like Phenotype and Their Pedigree Analysis

三个家族性高胆固醇血症样表型纯合子家系遗传异质性及其系谱分析

Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma

一个表皮松解性掌跖角化病家系的KRT9基因突变分析

By segregation analysis of recessive inheritance, 23 cases of 12 pedigree suffering from spinal muscular atrophy fit autosomal recessive inheritance.

隐性遗传分离分析表明，12个家系23例患儿发病方式符合常染色体隐性遗传。

Molecular genetic analysis for a pedigree with severe hereditary coagulation factor ⅶ deficiency

重型遗传性凝血因子Ⅶ缺陷症家系分子遗传学分析

Clinical and genetic analysis of a severe vWD pedigree

一个重症vWD家系临床与基因分析

A study on TSH receptor gene mutations in one child with congenital hypothyroidism and analysis of the pedigree

TSH受体基因突变致先天性甲状腺功能减退症一例及其家系分析