Confined to a wheelchair by haemophilia, he graduated from Shanghai's Jiaotong University in accountancy through a home study programme. 因患血友病而身陷轮椅的他通过自学,从上海交通大学会计学专业毕业。
Analysis of Intron 1 and Intron 22 Inversion in Factor ⅷ Gene in Patients with Haemophilia A 血友病A患者FⅧ基因内含子1及22倒位分析
Study on Bcll RFLP in Factor VIII Gene and Prenatal Diagnosis of Haemophilia A through RFLP 凝血因子Ⅷ基因内BclⅠ多态性的研究及其在甲型血友病产前基因诊断中的应用
Molecular Diagnosis of Haemophilia A: Analysis of Factor ⅷ Gene Rearrangements 血友病A的分子诊断:因子Ⅷ基因重排分析
Haemophilia A is one of the most common severe hereditary hemorrhagic disorders with an incidence rate of about 1,/ 10,000 among male neonates. 血友病A是人类最常见的遗传性出血性疾病,大约10000名出生男婴中有一人受累。
Haemophilia A is the most common inherited bleeding disorder in human, which is caused by deficiency in factor ⅷ( F ⅷ). 血友病甲是一种常见的遗传性出血性疾病,由因子FⅧ缺乏引起。
Haemophilia b is a kind of serious cruor-defective inhering diseaes. 血友病B是一种严重的凝血功能缺陷遗传病,由于现行的治疗方法对血友病B的治疗效果均不令人满意。
Haemophilia Bleeding into Muscles of Limbs& A Clinical Analysis of 61 Cases 61例血友病肌肉出血临床分析
Characterization of Genetic Defects in 73 Cases of Haemophilia A of Chinese Origin 73例中国人血友病甲基因突变的分析
Objective To establish the linkage methods of Xba ⅰ polymorphisms specific for F ⅷ gene intron 22, and to find a rapid and simple system for haemophilia A ( HA) carrier detection and prenatal diagnosis. 目的建立凝血因子Ⅷ(FⅧ)基因内含子22的XbaⅠ多态位点高特异的基因连锁分析法,并应用于血友病A(HA)家系中孕妇携带者检测及产前基因诊断。