1.
Inherited Dysfibrinogenemia Caused by Arg19Gly in theαChain of Fibrinogen
一个纤维蛋白原α链Arg 19 Gly突变导致的遗传性异常纤维蛋白原血症家系
2.
acquired fibrinogenemia
获得性纤维蛋白原血症
3.
The Researches on the Phenotypes and the Pathological Mechanisms of Congenital Afibrinogenemia;
遗传性无纤维蛋白原血症表型及病理机制的研究
4.
Genetic Analysis of an Inherited Afibrinogenemia Family Caused by a Novel Frameshift Mutation in FGA
一个新的FGA突变导致的遗传性无纤维蛋白原血症家族的分析
5.
The incidence, distribution and genetic polymorphism of the abnormal hemoglobin in China
我国异常血红蛋白发生率、分布及遗传多态性
6.
congenital afibrinogenemia
先天性纤维蛋白原缺乏症
7.
RELATIONSHIP BETWEEN SIMPLE OBESITY AND FIBRINOGEN GENE POLYMORPHISM IN CHILDREN;
儿童单纯性肥胖与纤维蛋白原基因遗传多态性的关联研究
8.
Fibrin and platelets combine to form a clot. Hemophilia is caused by a hereditary lack of one of the clotting factors.
血纤维蛋白和血小板一起形成血栓。血友病就是因为遗传上缺乏一种凝血胶原引起的。
9.
The incidence、distributing and genedc polymorphism of the abnormal hemoglobin in china minority
我国少数民族异常血红蛋白发生率、分布及遗传多态性
10.
hereditary enamel dysplasia
遗传性釉质发育异常症
11.
Analysis of high-sensitivity C-reactive protein,homocysteine,fibrinogen and serum lipid components in patients with silent cerebral infarction
无症状性脑梗死患者高敏C-反应蛋白、同型半胱氨酸、纤维蛋白原和血脂成分分析
12.
A study on the relation of plasma fibrinogen in patients with ischemic cerebrovascular disorder
缺血性脑卒中与血浆纤维蛋白原的相关性分析
13.
fibrinous pericarditis
血纤维蛋白性心包炎
14.
Perhaps the most thoroughly analyzed hereditary disease are those in which abnormal hemoglobin molecules are produced.
也许最详尽分析过的遗传性的疾病，乃是那些产生异常血红蛋白的遗传
15.
The inactive precursor to plasmin that is found in body fluids and blood plasma.
血纤维蛋白溶酶原血纤维蛋白溶酶不活跃的前体，常发现于体液和血浆中
16.
Study on the Specificity of Fibrinogen for the Postmortem Diagnosis of Myocardial Infarction;
纤维蛋白原在心肌梗死死后诊断的特异性研究
17.
The -148C/T Polymorphism of β-Fibrinogen Gene and Plasma Fibrinogen Levels in Young Adults with Ischemic Stroke;
青年缺血性卒中患者纤维蛋白原β-148C/T基因多态性和血浆纤维蛋白原水平研究
18.
Association Of Fibrinogen B P Gene Polymorphism With Plasma Fibrinogen Level In Coronary Heart Disease And Stroke;
心脑血栓性疾病纤维蛋白原Bβ链基因多态性与血浆纤维蛋白原的关系研究