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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.
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.
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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