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	1.	The highly prevalent deletions in F8 intron 13 found in French mild hemophilia A patients result from both founder effect and recurrent de novo events. [electronic resource] by Jourdy, Yohann Frétigny, Mathilde Lassalle, Fanny Lillicrap, David Négrier, Claude Vinciguerra, Christine Producer: 20210514 In: Journal of thrombosis and haemostasis : JTH vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Splicing analysis of 26 F8 nucleotide variations using a minigene assay. [electronic resource] by Jourdy, Yohann Fretigny, Mathilde Nougier, Christophe Négrier, Claude Bozon, Dominique Vinciguerra, Christine Producer: 20190429 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization. [electronic resource] by Jourdy, Yohann Janin, Alexandre Fretigny, Mathilde Lienhart, Anne Négrier, Claude Bozon, Dominique Vinciguerra, Christine Producer: 20181211 In: American journal of human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Algorithms using clinical and genetic data (CYP2C9, VKORC1) are relevant to predict warfarin dose in patients with different INR targets. [electronic resource] by Le Cam-Duchez, Véronique Frétigny, Mathilde Cailleux, Nicole Gandelin, Catherine Lévesque, Hervé Borg, Jeanne-Yvonne Producer: 20101228 In: Thrombosis research vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Molecular analysis of eight severe FV-deficient patients in Pakistan: A large series of homozygous for frameshift mutations. [electronic resource] by Borhany, Munira Ranc, Alexandre Fretigny, Mathilde Moulis, Grégory Abid, Madiha Shamsi, Tahir Giansily-Blaizot, Muriel Producer: 20200113 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Differential diagnosis of neonatal alloimmune thrombocytopenia: Type 2B von Willebrand disease. [electronic resource] by Penel-Page, Mathilde Meunier, Sandrine Fretigny, Mathilde Le Quellec, Sandra Boisseau, Pierre Vinciguerra, Christine Ternisien, Catherine Rugeri, Lucia Producer: 20180613 In: Platelets vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Severe hemophilia A caused by an unbalanced chromosomal rearrangement identified using nanopore sequencing. [electronic resource] by Chatron, Nicolas Schluth-Bolard, Caroline Frétigny, Mathilde Labalme, Audrey Vilchez, Gaëlle Castet, Sabine-Marie Négrier, Claude Sanlaville, Damien Vinciguerra, Christine Jourdy, Yohann Producer: 20200714 In: Journal of thrombosis and haemostasis : JTH vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort. [electronic resource] by Nurden, Alan T Pillois, Xavier Fiore, Mathieu Alessi, Marie-Christine Bonduel, Mariana Dreyfus, Marie Goudemand, Jenny Gruel, Yves Benabdallah-Guerida, Schéhérazade Latger-Cannard, Véronique Négrier, Claude Nugent, Diane Oiron, Roseline D Rand, Margaret L Sié, Pierre Trossaert, Marc Alberio, Lorenzo Martins, Nathalie Sirvain-Trukniewicz, Peggy Couloux, Arnaud Canault, Mathias Fronthroth, Juan Pablo Fretigny, Mathilde Nurden, Paquita Heilig, Roland Vinciguerra, Christine Producer: 20160112 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)