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	1.	A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH. [electronic resource] by Paoloni-Giacobino, A Lespinasse, J Moix, I Dahoun, S P Producer: 20020114 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	N-acetylcysteine augments adenovirus-mediated gene expression in human endothelial cells by enhancing transgene transcription and virus entry. [electronic resource] by Jornot, L Morris, M A Petersen, H Moix, I Rochat, T Producer: 20020426 In: The journal of gene medicine vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Effects of first generation E1E3-deleted and second generation E1E3E4-deleted/modified adenovirus vectors on human endothelial cell death. [electronic resource] by Jornot, L Petersen, H Lusky, M Pavirani, A Moix, I Rochat, T Producer: 20030711 In: Endothelium : journal of endothelial cell research vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl. [electronic resource] by Kollios, Konstantinos Tsolaki, Anastasia Antachopoulos, Charalampos Moix, I Morris, Michael A Papadopoulou, Maria Roilides, Emmanuel Producer: 20111024 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Phenotypic heterogeneity of dopa-responsive dystonia in monozygotic twins. [electronic resource] by Grötzsch, H Schnorf, H Morris, M A Moix, I Horvath, J Prilipko, O Burkhard, P R Producer: 20050121 In: Neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features. [electronic resource] by Makrythanasis, P Moix, I Gimelli, S Fluss, J Aliferis, K Antonarakis, S E Morris, M A Béna, F Bottani, A Producer: 20101207 In: Clinical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation. [electronic resource] by Djambas Khayat, C Salem, N Chouery, E Corbani, S Moix, I Nicolas, E Morris, M A de Moerloose, P Mégarbané, A Producer: 20090519 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Guidelines for the genetic diagnosis of hereditary recurrent fevers. [electronic resource] by Shinar, Y Obici, L Aksentijevich, I Bennetts, B Austrup, F Ceccherini, I Costa, J M De Leener, A Gattorno, M Kania, U Kone-Paut, I Lezer, S Livneh, A Moix, I Nishikomori, R Ozen, S Phylactou, L Risom, L Rowczenio, D Sarkisian, T van Gijn, M E Witsch-Baumgartner, M Morris, M Hoffman, H M Touitou, I Producer: 20121119 In: Annals of the rheumatic diseases vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)