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American Journal of Ophthalmology|May 15, 1987
Immunohistochemical characterization of human retinoblastomas in situ with multiple markersE Perentes, C P Herbort, L J Rubinstein, et al.
Neuro-Chirurgie|March 23, 2010
[Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1)]B Rilliet, B Pittet, D Montandon, et al.
The International Journal of Artificial Organs|December 6, 2003
Quantitative assessment of cell viability and apoptosis in cultured epidermal autografts: application to burn therapyM Vernez, W Raffoul, M C Gailloud-Matthieu, et al.
Investigative Ophthalmology & Visual Science|September 7, 1999
On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophiesE Korvatska, F L Munier, P Chaubert, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOXE Korvatska, F L Munier, L Zografos, et al.
Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1992
[Loss of ganglion cells in the retina secondary to vincristine therapy]F Munier, S Uffer, C P Herbort, et al.
Ophthalmic Genetics|March 1, 1997
Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastomaF L Munier, F Thonney, A Balmer, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1991
[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]F Munier, A Balmer, C von Moos, et al.
American Journal of Human Genetics|April 16, 1998
Mutation hot spots in 5q31-linked corneal dystrophiesE Korvatska, F L Munier, A Djemaï, et al.
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