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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 10, 2023. (Total: 217827Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Thrombophilia and F12[original query]
Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population.
Stroke; a journal of cerebral circulation 2004 Aug 35 (8): 1795-9.
Santamaría Amparo, Mateo José, Tirado Isabel, Oliver Arturo, Belvís Roberto, Martí-Fábregas Joan, Felices Rosa, Soria José Manuel, Souto Juan Carlos, Fontcuberta Jor
Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.
Thrombosis and haemostasis 2004 May 91 (5): 899-904.
Tirado Isabel, Soria José Manuel, Mateo José, Oliver Artur, Souto Juan Carlos, Santamaria Amparo, Felices Rosa, Borrell Montserrat, Fontcuberta Jor
Multiplex assay for genetic testing of thrombophilia: a method for routine clinical care.
Journal of clinical laboratory analysis 2007 21 (6): 349-55.
López Mónica, Giraldo Pilar, Alvarez Patricia, Cornudella R, Pocoví Miguel, Martínez Antonio, Fontcuberta Jordi, Soria José Manu
Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy.
Journal of thrombosis and haemostasis : JTH 2010 Apr 8 (4): 707-13.
Galanaud J P, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny J L, Mares P, Dauzat M, Quere I, Gris J
The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis.
BMC medical genetics 2018 Mar 19 (1): 50.
Wu Xi, Ding Qiulan, Wang Xuefeng, Dai Jing, Wu Wenm
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