L'art ou la consistance du jeu in Etudes canadiennes. Canadian StudiesBERNIER, L; PERRAULT, I.Loisir et société. 1985, Vol 8, Num 2, pp 659-664, issn 0705-3436Article

Structure and refinement of the physical mapping of the γ-glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesotheliomaROZET, J.-M; GERBER, S; PERRAULT, I et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 1-2, pp 91-94, issn 0301-0171Conference Paper

Age-related macular degeneration in grandparents of patients with Stargardt disease : Genetic studySOUIED, E. H; DUCROQ, D; KAPLAN, J et al.American journal of ophthalmology. 1999, Vol 128, Num 2, pp 173-178, issn 0002-9394Article

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and stargardt disease: evidence of clinical heterogeneity at this locusROZET, J.-M; GERBER, S; GHAZI, I et al.Journal of medical genetics. 1999, Vol 36, Num 6, pp 447-451, issn 0022-2593Article

Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophyKELSELL, R. E; GREGORY-EVANS, K; PAYNE, A. M et al.Human molecular genetics (Print). 1998, Vol 7, Num 7, pp 1179-1184, issn 0964-6906Article

L'autre sociologie : approches qualitatives de la réalité socialeLAPERRIERE, A; CHANFRAULT-DUCHET, M. F; BERNIER, L et al.Cahiers de Recherche Sociologique. 1987, Vol 5, Num 2, pp 5-138Article

Amaurose congénitale de Leber : le point sur l'hétérogénéité génétique, actualisation de la définition clinique : Rétinopathies pigmentaires = Leber congenital amaurosis: comprehensive survey of genetic heterogeneity. A clinical definition update : Retinitis pigmentosaHANEIN, S; PERRAULT, I; GERBER, S et al.Journal français d'ophtalmologie. 2005, Vol 28, Num 1, pp 98-105, issn 0181-5512, 8 p.Article

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3CABOT, A; ROZET, J.-M; GERBER, S et al.American journal of human genetics. 1999, Vol 64, Num 4, pp 1141-1146, issn 0002-9297Article

Exclusion of five subunits of cGMP phosphodiesterase in Leber's congenital amaurosisPERRAULT, I; CHATELIN, S; KAPLAN, J et al.Human genetics. 1998, Vol 102, Num 3, pp 322-326, issn 0340-6717Article

Severe manifestions in carrier females in X linked retinitis pigmentosaSOUIED, E; SEGUES, B; DUFIER, J.-L et al.Journal of medical genetics. 1997, Vol 34, Num 10, pp 793-797, issn 0022-2593Article