遗传性

CuNiFe合金在特殊涂层中的深过冷及其遗传性

High undercooling and heredity of Cu - Ni - Fe alloys in special coating materials

钢中过热断口遗传性的SEM研究

SEM investigation on fracture heredity in overheated steel

肥胖往往有遗传性。

Fatness tends to run in families .

湿疹是一种常见的皮肤病，通常具遗传性。

Eczema is a common skin complaint which often runs in families .

口吃很可能是一种遗传性缺陷。

Stammering is probably an inherited defect .

人类的长寿具有家族遗传性。

Human longevity runs in families

那是一种遗传性疾病。

It 's a genetic disease .

这就是遗传性缺陷。

This is the genetic defects .

这些特征是遗传性的，如眼的颜色和脚丫子的大小，这都是你所无法驾驭的。

These traits are hereditary , like eye color or foot size , and there 's nothing you can do to change them .

所有的患儿体表有超过20%的遗传性过敏症皮炎感染

All of the children had atopic dermatis coercing at least 20 % of their body surface area .

西南地区母系遗传性耳聋家系的线粒体DNA分析

Mitochondrial DNA Mutations in Matrilineal Nonsyndromic Deafness Pedigrees of Southwest China

A（c1）温度以下加热速度对钢的组织遗传性影响

Influences of Heating Rate under A_ ( c_1 ) of Steel on the Structural Inheritance

也可以破坏遗传性卵巢癌病毒染色体（DNA）。

Also can damage the hereditary ovarian cancer virus chromosome ( DNA ) .

遗传性凝血因子V缺陷症的实验室诊断

Laboratory diagnosis of a pedigree with congenital coagulation factor V deficiency

铝合金中Fe相形态的遗传性及球化机制的研究

The heredity of iron compound morphologies in Al alloys and spheroidizing mechanism

应用精子载体法导入外源DNA影响家蚕遗传性的研究

Study on Effect of External DNA Introduction by Sperm Vector Method on Inheritance of the Silkworm , Bombyx mori

2种新的凝血因子V基因突变导致的遗传性凝血因子V缺乏症

Two novel factor V gene mutations associated with congenital coagulation factor V deficiency , study of one pedigree

遗传性视网膜变性rd小鼠及其感光细胞凋亡研究

Hereditary retinal dystrophy of rd mice and photoreceptors apoptosis

遗传性IgM肾病一家系三例报告及文献复习

Hereditary IgM nephropathy : report of three cases in a kindred and review of literatures

方法回顾分析5例经临床、X线平片及CT检查，且手术病理证实为遗传性多发性骨软骨瘤恶变的影像学表现。

Methods A retrospective analysis was done in 5 cases with canceration of hereditary multiple osteochondroma that were proved by operative histology , X ray and CT scanning .

结节性硬化综合症（TuberousSclerosisComplex，TSC），是一种以全身多器官错构瘤病变为特征的常染色体显性遗传性疾病。

Tuberous sclerosis complex ( TSC ) is an autosomal dominant disorder characterized by hamartomas in the affected organs .

FG与遗传性非息肉性结肠直肠癌综合征

Fordyce granules and hereditary non-polyp-osis colorectal cancer syndrome

Leber遗传性视神经病变mtDNA新原发突变位点研究

New primary mutation of mtDNA in Leber ′ s hereditary optic neuropathy

MDS的细胞遗传性克隆性异常可以指导中医的辨证分型及临床治疗。

MDS clonal cell genetic abnormalities can guide the dialectical traditional Chinese medicine classification and clinical treatment .

结论（1）PMD是一种常见的遗传性肌源性疾病，其中DMD最常见；

Conclusion ( 1 ) PMD is a common genetically determined myopathy . DMD is the most common .

遗传性肾炎（Alport综合征）&一个家系的调查报告

Hereditary nephritis ( alport 's syndrome ) & on an of pedigree

遗传性平衡易位t（3；22）（p21；q13）家系

Hereditary Balanced Translocation t ( 3 ; 22 ) ( p21 ; q13 ) Pedigree

G6PD是磷酸戊糖旁路代谢的限速酶，也是重要的看家酶.G6PD缺乏症是人类常见的遗传性疾病。

Glucose-6-phosphate dehydrogenase ( G6PD ) is the key enzyme of Pentose Phosphate Pathway , G6PD deficiency is common hereditary disease .

遗传性LQTS致病基因的突变也与很多普通药物诱导的LQTS相关。

Mutations in genes for inherited LQTS are also associated with much more common drug-induced LQTS .

HFE蛋白与遗传性血色病

HFE protein and hereditary haemochromatosis