Munier FL - Search Results

1

Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy.

Ren Z, Lin PY, Klintworth GK, Iwata F, Munier FL, Schorderet DF, El Matri L, Theendakara V, Basti S, Reddy M, Hejtmancik JF. Ren Z, et al. Among authors: munier fl. Hum Genet. 2002 Jun;110(6):568-77. doi: 10.1007/s00439-002-0729-z. Epub 2002 Apr 20. Hum Genet. 2002. PMID: 12107443

2

Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21.

Héon E, Piguet B, Munier F, Sneed SR, Morgan CM, Forni S, Pescia G, Schorderet D, Taylor CM, Streb LM, Wiles CD, Nishimura DY, Sheffield VC, Stone EM. Héon E, et al. Arch Ophthalmol. 1996 Feb;114(2):193-8. doi: 10.1001/archopht.1996.01100130187014. Arch Ophthalmol. 1996. PMID: 8573024

3

Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.

Munier FL, Thonney F, Balmer A, Héon E, Pescia G, Schorderet DF. Munier FL, et al. Klin Monbl Augenheilkd. 1996 May;208(5):400-3. doi: 10.1055/s-2008-1035252. Klin Monbl Augenheilkd. 1996. PMID: 8766064

4

[Oncogenes and anti-oncogenes: the genetics of cancer].

Schorderet DF, Munier FL. Schorderet DF, et al. Among authors: munier fl. Praxis (Bern 1994). 1996 Aug 27;85(35):1019-22. Praxis (Bern 1994). 1996. PMID: 8848670 French.

5

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 LOX.

Korvatska E, Munier FL, Zografos L, Ahmad F, Faggioni R, Dolivo-Beuret A, Uffer S, Pescia G, Schorderet DF. Korvatska E, et al. Among authors: munier fl. Eur J Hum Genet. 1996;4(4):214-8. doi: 10.1159/000472201. Eur J Hum Genet. 1996. PMID: 8875187

6

Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene.

Piguet B, Héon E, Munier FL, Grounauer PA, Niemeyer G, Butler N, Schorderet DF, Sheffield VC, Stone EM. Piguet B, et al. Among authors: munier fl. Ophthalmic Genet. 1996 Dec;17(4):175-86. doi: 10.3109/13816819609057891. Ophthalmic Genet. 1996. PMID: 9010868

7

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies.

Munier FL, Korvatska E, Djemaï A, Le Paslier D, Zografos L, Pescia G, Schorderet DF. Munier FL, et al. Nat Genet. 1997 Mar;15(3):247-51. doi: 10.1038/ng0397-247. Nat Genet. 1997. PMID: 9054935

8

Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma.

Munier FL, Thonney F, Balmer A, Uffer S, Héon E, Van Melle G, Rutz HP, Pescia G, Schorderet DF. Munier FL, et al. Ophthalmic Genet. 1997 Mar;18(1):7-12. doi: 10.3109/13816819709057878. Ophthalmic Genet. 1997. PMID: 9134545

9

Mutation hot spots in 5q31-linked corneal dystrophies.

Korvatska E, Munier FL, Djemaï A, Wang MX, Frueh B, Chiou AG, Uffer S, Ballestrazzi E, Braunstein RE, Forster RK, Culbertson WW, Boman H, Zografos L, Schorderet DF. Korvatska E, et al. Among authors: munier fl. Am J Hum Genet. 1998 Feb;62(2):320-4. doi: 10.1086/301720. Am J Hum Genet. 1998. PMID: 9463327 Free PMC article.

10

[Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)].

Lefèvre A, Hiroz C, Zografos L, Schorderet DF, Munier FL. Lefèvre A, et al. Among authors: munier fl. Klin Monbl Augenheilkd. 1998 May;212(5):301-4. Klin Monbl Augenheilkd. 1998. PMID: 9677562 French.

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