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Showing results (11-20 of 21) with videos related to

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Nature Genetics|June 1, 1992
Detection of over 98% cystic fibrosis mutations in a Celtic populationC Férec, M P Audrezet, B Mercier, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Novel mutations in the duplicated region of PKD1 geneR Perrichot, B Mercier, I Quere, et al.
La Revue De Medecine Interne|September 3, 2003
[A common mutation C677T in the 5,10-methyltetrahydrofolate reductase gene is associated to idiopathic deep venous thrombosis]G Berrut, A Ghali, I Quere, et al.
Journal of Thrombosis and Haemostasis : JTH|October 2, 2009
Comparison of the clinical history of symptomatic isolated distal deep-vein thrombosis vs. proximal deep vein thrombosis in 11 086 patientsJ P Galanaud, S Quenet, K Rivron-Guillot, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Superficial vein thrombosis and recurrent venous thromboembolism: a pooled analysis of two observational studiesJ P Galanaud, J L Bosson, C Genty, et al.
Clinical Genetics|March 22, 2001
Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitisJ M Chen, A Piepoli Bis, L Le Bodic, et al.
Journal of Thrombosis and Haemostasis : JTH|January 24, 2014
Incidence and predictors of venous thromboembolism recurrence after a first isolated distal deep vein thrombosisJ-P Galanaud, M-A Sevestre, C Genty, et al.
Journal of Thrombosis and Haemostasis : JTH|February 10, 2010
Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancyJ P Galanaud, E Cochery-Nouvellon, S Alonso, et al.
Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.
Presse Medicale (Paris, France : 1983)|March 31, 2005
[Therapeutic intensification and autologous stem cell transplantation in autoimmune diseases]Z Marjanovic, I Gerber, C Toledano, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Nature Genetics|June 1, 1992
Detection of over 98% cystic fibrosis mutations in a Celtic populationC Férec, M P Audrezet, B Mercier, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Novel mutations in the duplicated region of PKD1 geneR Perrichot, B Mercier, I Quere, et al.
La Revue De Medecine Interne|September 3, 2003
[A common mutation C677T in the 5,10-methyltetrahydrofolate reductase gene is associated to idiopathic deep venous thrombosis]G Berrut, A Ghali, I Quere, et al.
Journal of Thrombosis and Haemostasis : JTH|October 2, 2009
Comparison of the clinical history of symptomatic isolated distal deep-vein thrombosis vs. proximal deep vein thrombosis in 11 086 patientsJ P Galanaud, S Quenet, K Rivron-Guillot, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Superficial vein thrombosis and recurrent venous thromboembolism: a pooled analysis of two observational studiesJ P Galanaud, J L Bosson, C Genty, et al.
Clinical Genetics|March 22, 2001
Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitisJ M Chen, A Piepoli Bis, L Le Bodic, et al.
Journal of Thrombosis and Haemostasis : JTH|January 24, 2014
Incidence and predictors of venous thromboembolism recurrence after a first isolated distal deep vein thrombosisJ-P Galanaud, M-A Sevestre, C Genty, et al.
Journal of Thrombosis and Haemostasis : JTH|February 10, 2010
Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancyJ P Galanaud, E Cochery-Nouvellon, S Alonso, et al.
Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.
Presse Medicale (Paris, France : 1983)|March 31, 2005
[Therapeutic intensification and autologous stem cell transplantation in autoimmune diseases]Z Marjanovic, I Gerber, C Toledano, et al.
Pageof 3