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American College of Medical Genetics consensus statement on factor V Leiden mutation testing.

作者信息

Grody W W, Griffin J H, Taylor A K, Korf B R, Heit J A

机构信息

Divisions of Medical Genetics and Molecular Pathology, UCLA School of Medicine, Los Angeles, California, USA.

出版信息

Genet Med. 2001 Mar-Apr;3(2):139-48. doi: 10.1097/00125817-200103000-00009.

DOI:10.1097/00125817-200103000-00009
PMID:11280951
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3111091/
Abstract
摘要

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本文引用的文献

1
Prevalence of factor V Leiden and prothrombin variant G20210A in patients age <50 years with no significant stenoses at angiography three to four weeks after myocardial infarction.心肌梗死后三至四周行血管造影无明显狭窄的50岁以下患者中因子V莱顿突变和凝血酶原变异体G20210A的患病率。
J Am Coll Cardiol. 2000 Sep;36(3):717-22. doi: 10.1016/s0735-1097(00)00772-5.
2
The HR2 haplotype of factor V: effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis.凝血因子V的HR2单倍型：对凝血因子V水平、标准化活化蛋白C敏感率及静脉血栓形成风险的影响
Thromb Haemost. 2000 Apr;83(4):577-82.
3
The factor V R2 allele: risk of venous thromboembolism, factor V levels and resistance to activated protein C.
Thromb Haemost. 2000 Feb;83(2):204-8.
4
Risk factors for deep vein thrombosis and pulmonary embolism: a population-based case-control study.深静脉血栓形成和肺栓塞的危险因素：一项基于人群的病例对照研究。
Arch Intern Med. 2000 Mar 27;160(6):809-15. doi: 10.1001/archinte.160.6.809.
5
Predictors of recurrence after deep vein thrombosis and pulmonary embolism: a population-based cohort study.深静脉血栓形成和肺栓塞后复发的预测因素：一项基于人群的队列研究。
Arch Intern Med. 2000 Mar 27;160(6):761-8. doi: 10.1001/archinte.160.6.761.
6
Inherited thrombophilia and pregnancy loss.
Thromb Haemost. 1999 Aug;82(2):634-40.
7
Heritable coagulopathies in pregnancy.妊娠期遗传性凝血障碍
Obstet Gynecol Surv. 1999 Dec;54(12):754-65. doi: 10.1097/00006254-199912000-00004.
8
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden).
Blood. 1999 Nov 1;94(9):3062-6.
9
The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation.凝血因子V Leiden和凝血酶原G20210A突变的杂合携带者发生复发性深静脉血栓形成的风险。
N Engl J Med. 1999 Sep 9;341(11):801-6. doi: 10.1056/NEJM199909093411104.
10
Non-PCR-dependent detection of the factor V Leiden mutation from genomic DNA using a homogeneous invader microtiter plate assay.使用均相侵入式微孔板分析法从基因组DNA中进行不依赖聚合酶链反应的因子V莱顿突变检测。
Mol Diagn. 1999 Jun;4(2):135-44. doi: 10.1016/s1084-8592(99)80037-x.