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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

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

Performance of electrolyte assays in the United Kingdom-reference target valuesTHOMAS, M. A; SMITH, S. C; SALL, S et al.Accreditation and quality assurance. 2004, Vol 9, Num 3, pp 159-163, issn 0949-1775, 5 p.Conference Paper

Human cytomegalovirus-infected cells have unstable assembly of major histocompatibility complex class I complexes and are resistant to lysis by cytotoxic T lymphocytesWARREN, A. P; DUCROQ, D. H; LEHNER, P. J et al.Journal of virology. 1994, Vol 68, Num 5, pp 2822-2829, issn 0022-538XArticle