1. Characterization of five associations of F8 missense mutations containing FVIII B domain mutations. (25th February 2016) Authors: Jourdy, Y.; Nougier, C.; Roualdes, O.; Fretigny, M.; Durand, B.; Negrier, C.; Vinciguerra, C. Journal: Haemophilia Issue: Volume 22:Number 4(2016:Jul.) Page Start: 583 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Characterization of four novel molecular changes in the promoter region of the factor VIII gene. (30th December 2013) Authors: Nougier, C.; Roualdes, O.; Fretigny, M.; d'Oiron, R.; Costa, C.; Negrier, C.; Vinciguerra, C. Journal: Haemophilia Issue: Volume 20:Number 2(2014:Mar.) Page Start: e149 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Characterization of four novel molecular changes in the promoter region of the factor VIII gene. (30th December 2013) Authors: Nougier, C.; Roualdes, O.; Fretigny, M.; d'Oiron, R.; Costa, C.; Negrier, C.; Vinciguerra, C. Journal: Haemophilia Issue: Volume 20:Number 2(2014:Mar.) Page Start: e149 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiency. (24th February 2015) Authors: Roualdes, O.; Nougier, C.; Fretigny, M.; Talagrand, E.; Durand, B.; Negrier, C.; Vinciguerra, C. Journal: Haemophilia Issue: Volume 21:Number 3(2015:May) Page Start: e202 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗