佳学基因对Factor V Leiden易栓症的发生进行了基因解码,并将之收入《人的基因序列变化与人体疾病表征》中,便于医生选择和使用,进行Factor V Leiden易栓症遗传阻断,也便于患者更好地进行治疗和健康管理。 Factor V Leiden易栓症疾病介绍: Factor V Leiden易栓症是一种遗传性血液凝固障碍。Factor V Leiden是导致易...
The meaning of FACTOR V LEIDEN is a point mutation producing an abnormal version of factor V that is resistant to inactivation and causes prolonged clotting of blood.
Factor V Leiden deficiency?doi:10.1111/j.1651-2227.2002.tb00116.xK McFaddenK McFaddenActa Paediatrica
FactorVLeiden易栓症是英文factor V Leiden thrombophilia的中文翻译。这一疾病又叫做facio-scapulo-humeral dystrophyfacioscapulohumeral atrophyfacioscapulohumeral type progressive muscular dystrophyfacioscapuloperoneal muscular dystrophyFSH muscular dystrophyFSHDmuscular dystrophy, facioscapulohumeral;。该病是一种基因...
appointed Assistant Professor at Harvard University in 1994 and Professor at Leiden University, the Netherlands in 1998. shawprize.org 于1990年至1994年间,她曾在不同学院从事博士后研究,其中包括哈佛史密森天体物理中心、加州大学柏 克莱分校和斯坦福大学,1994年被委任为哈佛大学助理教授及1998年为 荷 兰 莱...
Individuals with a positive screening assay should have the DNA test for confirmation and to distinguish heterozygotes, homozygotes, and "pseudohomozygotes" who are heterozygous for both Factor V Leiden and a second mutation causing Factor V deficiency. When relatives of individuals known to have ...
Factor V Leiden (FVL) and the c . 97G > A mutation in the 3鈥 untranslated region of the prothrombin gene are the most common inherited causes of thrombophilia. FVL results in resistance to activated protein C (APC cleavage), while c . 97G > A leads to increased prothrombin production...
Free Essays from Bartleby | Factor V Leiden Thrombophilia Thrombophilia is a disorder that contains several genetic components that can cause an individual...
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Standen GR, Morse C et al.DVT following oral contraceptive therapy in association with homozygous factor V Leiden. Aslam S. Clinical and Laboratory Haematology . 1995Aslam S.Standen GR, Morse C et al.DVT following oral contraceptive therapy in association with homozygous factor V Leiden.Clinical ...