1.
Identification of Gene Mutations Involved in Five Cases of Inherited Coagulation Factor V Deficiency;
五例遗传性凝血因子V缺乏症的基因分析
2.
Study on Molecular Pathology of Inheritary Deficiency of Factor V and Phenotype of 2A Type Von Wil Lebrand Disease;
遗传性凝血因子V缺乏症分子病理机制的研究和2A型vWD的临床研究
3.
coagulation factor deficiency
凝血因子缺乏性疾病
4.
Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI.
在典型的血友病中缺乏的是凝血因子VIII;其它的血友病是因缺乏凝血因子IX或XI。
5.
The Clinical Aspects and Molecule Mechanisms of Congenital Coagulation Factor V Deficiency: Studies of Two Families;
两个先天性凝血因子V缺陷症家系的临床和分子发病机制研究
6.
Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.
血友病: 一种遗传性出血性疾病,因先天性缺乏某种凝血因子而引起。
7.
The correlation of antiphospholipid antibody and factor Ⅻ deficiency in patients with retinal vein occlusion
抗磷脂抗体及凝血因子Ⅻ缺乏与视网膜静脉阻塞的相关研究
8.
congenital aprothrombinemia
先天性凝血酶原缺乏症
9.
hemophilia caused by a congenital deficiency of factor VIII; occurs almost exclusively in men.
由于先天缺乏凝血银子VIII而引起的血友病；通常出现在男性。
10.
a clotting disorder similar to hemophilia A but caused by a congenital deficiency of factor IX.
凝固混乱由于缺乏凝固银子IX。
11.
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。
12.
Preclinical Research of Inherited Anti-coagulation Factor and Acquired Coagulation Factor Deficiency;
遗传性抗凝因子和获得性凝血因子缺陷症的基础研究
13.
The whites of his eyes were bloodshot from lack of sleep.
他的眼白因缺乏睡眠而充满血丝。
14.
Studies on Deficiency Detection and SNPs of Exon 12 of Plasma Thromboplastin Antecedent Gene in Bovine;
牛凝血因子XI基因缺陷病检测及其第12外显子SNPs分析
15.
Through the failure, absence, or lack of.
因缺少，在缺乏…时因为不足、缺少或缺乏
16.
Scurvy (or vitamin C deficiency)：Nutritional disorder caused by deficiency of vitamin C.
坏血病(亦称维生素c缺乏病):因维生素c缺乏而引起的营养性疾病。
17.
Finite Element Analyses of Stress Intensity Factors of Cracks at V-Notches
V型缺口根部裂纹应力强度因子的有限元分析
18.
Identification of a Novel Deletion Mutation of F13A Gene in a Pedigree with Factor XIII Deficiency;
一种新的凝血因子XIII基因突变导致的遗传性FXIII缺陷症