Method of screening for the presence of a genetic defect associated with deep venous thrombosis

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Nov 29, 2011
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Oct 29, 2009
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Mar 31, 2006
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Apr 1, 2005

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Abstract

A. The genetic marker comprises a set of one, two, three or four mutations in the nucleic acid material encoding fibrinogen γ, the mutations being selected from the group consisting of 129A/T (rs2066854), 7874G/A (rs20668β1), 9615′C/T (rs2066864) and 10034C/T (rs2066865).

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BIOMERIEUX B V	5280 AB BOXTEL

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Inventor Name	Address	# of filed Patents	Total Citations
Bertina, Rogier Maria	Leiden, NL	8	25
Henrica, de Visser-van Soest Maria Catharina	Leiderdorp, NL	1	0
Rosendaal, Frits R	Wassenaar, NL	15	58
Uitte, de Willige Shirley	Leeds, GB	1	0
Vos, Hans Luuk	Bodegraven, NL	1	0

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Method of screening for the presence of a genetic defect associated with deep venous thrombosis

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United States of America Patent

11887495

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PATENT NO	8067209
APP PUB NO	20090269738A1
SERIAL NO	11887495
DOCKET NO

US Family Size	Non-US Coverage
Patent Longevity	Forward Citations

DATE PUBLISHED	PUBLICATION/PATENT NO.	PUBLICATION TYPE
November 29, 2011	US,8067209,B2 US8067209B2	GRANTED PATENT AS SECOND PUBLICATION
October 29, 2009	US,20090269738,A1 US20090269738A1	FIRST PUBLISHED PATENT APPLICATION

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11887495

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