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	21.	The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103. [electronic resource] by Neerman-Arbez, M Antonarakis, S E Blouin, J L Zeinali, S Akhtari, M Afshar, Y Tuddenham, E G Producer: 19970826 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	The GM2-1 ganglioside islet autoantigen in insulin-dependent diabetes mellitus is expressed in secretory granules and is not beta-cell specific. [electronic resource] by Dotta, F Previti, M Neerman-Arbez, M Dionisi, S Cucinotta, D Lenti, L Di Mario, U Halban, P A Producer: 19980115 In: Endocrinology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations. [electronic resource] by Casini, A Lukowski, S Quintard, V Louvain Crutu, A Zak, M Regazzoni, S de Moerloose, P Neerman-Arbez, M Producer: 20150414 In: Thrombosis research vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia. [electronic resource] by Casini, A Vilar, R Beauverd, Y Aslan, D Devreese, K Mondelaers, V Alberio, L Gubert, C de Moerloose, P Neerman-Arbez, M Producer: 20180319 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Des-(27-31)C-peptide. A novel secretory product of the rat pancreatic beta cell produced by truncation of proinsulin connecting peptide in secretory granules. [electronic resource] by Verchere, C B Paoletta, M Neerman-Arbez, M Rose, K Irminger, J C Gingerich, R L Kahn, S E Halban, P A Producer: 19961226 In: The Journal of biological chemistry vol. 271 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency. [electronic resource] by Neerman-Arbez, M Johnson, K M Morris, M A McVey, J H Peyvandi, F Nichols, W C Ginsburg, D Rossier, C Antonarakis, S E Tuddenham, E G Producer: 19990419 In: Blood vol. 93 Availability: No items available. Save to lists Add to cart (remove)
	27.	In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes. [electronic resource] by Stroka, D Keogh, A Vu, D Fort, A Stoffel, M H Kühni-Boghenbor, K Furer, C Banz, V Demarmels Biasiutti, F Lämmle, B Candinas, D Neerman-Arbez, M Producer: 20151015 In: Journal of thrombosis and haemostasis : JTH vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia. [electronic resource] by Neerman-Arbez, M de Moerloose, P Bridel, C Honsberger, A Schönbörner, A Rossier, C Peerlinck, K Claeyssens, S Di Michele, D d'Oiron, R Dreyfus, M Laubriat-Bianchin, M Dieval, J Antonarakis, S E Morris, M A Producer: 20000810 In: Blood vol. 96 Availability: No items available. Save to lists Add to cart (remove)
	29.	Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. [electronic resource] by Neerman-Arbez, M de Moerloose, P Honsberger, A Parlier, G Arnuti, B Biron, C Borg, J Y Eber, S Meili, E Peter-Salonen, K Ripoll, L Vervel, C d'Oiron, R Staeger, P Antonarakis, S E Morris, M A Producer: 20010531 In: Human genetics vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)