Morlé L - Search Results

1

Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome 15q12-q15 and refinement to a 4.4 Mb region.

Michon L, Morlé L, Bozon M, Duret L, Zech JC, Godet J, Plauchu H, Edery P. Michon L, et al. Among authors: morle l. Eur J Hum Genet. 2004 Jul;12(7):574-8. doi: 10.1038/sj.ejhg.5201197. Eur J Hum Genet. 2004. PMID: 15083168

2

Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

Alloisio N, Morlé L, Bozon M, Godet J, Verhoeven K, Van Camp G, Plauchu H, Muller P, Collet L, Lina-Granade G. Alloisio N, et al. Among authors: morle l. Eur J Hum Genet. 1999 Feb-Mar;7(2):255-8. doi: 10.1038/sj.ejhg.5200273. Eur J Hum Genet. 1999. PMID: 10196713

3

A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss.

Morlé L, Bozon M, Alloisio N, Latour P, Vandenberghe A, Plauchu H, Collet L, Edery P, Godet J, Lina-Granade G. Morlé L, et al. J Med Genet. 2000 May;37(5):368-70. doi: 10.1136/jmg.37.5.368. J Med Genet. 2000. PMID: 10807696 Free PMC article.

4

A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

Morlé L, Bozon M, Zech JC, Alloisio N, Raas-Rothschild A, Philippe C, Lambert JC, Godet J, Plauchu H, Edery P. Morlé L, et al. Am J Hum Genet. 2000 Dec;67(6):1592-7. doi: 10.1086/316894. Epub 2000 Oct 13. Am J Hum Genet. 2000. PMID: 11035633 Free PMC article.

5

Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24.

Verot L, Alloisio N, Morlé L, Bozon M, Touraine R, Plauchu H, Edery P. Verot L, et al. Among authors: morle l. Am J Med Genet A. 2003 Sep 15;122A(1):37-41. doi: 10.1002/ajmg.a.20221. Am J Med Genet A. 2003. PMID: 12949969

6

New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia.

Beby F, Commeaux C, Bozon M, Denis P, Edery P, Morlé L. Beby F, et al. Among authors: morle l. Arch Ophthalmol. 2007 Feb;125(2):213-6. doi: 10.1001/archopht.125.2.213. Arch Ophthalmol. 2007. PMID: 17296897

7

Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14.

Zech JC, Morlé L, Vincent P, Alloisio N, Bozon M, Gonnet C, Milazzo S, Grange JD, Trepsat C, Godet J, Plauchu H. Zech JC, et al. Among authors: morle l. Graefes Arch Clin Exp Ophthalmol. 1999 May;237(5):387-93. doi: 10.1007/s004170050249. Graefes Arch Clin Exp Ophthalmol. 1999. PMID: 10333105

8

Novel VCAN mutations and evidence for unbalanced alternative splicing in the pathogenesis of Wagner syndrome.

Kloeckener-Gruissem B, Neidhardt J, Magyar I, Plauchu H, Zech JC, Morlé L, Palmer-Smith SM, Macdonald MJ, Nas V, Fry AE, Berger W. Kloeckener-Gruissem B, et al. Among authors: morle l. Eur J Hum Genet. 2013 Mar;21(3):352-6. doi: 10.1038/ejhg.2012.137. Epub 2012 Jun 27. Eur J Hum Genet. 2013. PMID: 22739342 Free PMC article.

9

[Genetic deafness:the primary cause of sensorineural hearing loss in children].

Lina-Granade G, Morlé L, Alloisio N, Edery P, Plauchu H, Truy E, Disant F, Collet L. Lina-Granade G, et al. Among authors: morle l. Arch Pediatr. 2001 Mar;8(3):308-12. doi: 10.1016/s0929-693x(00)00201-3. Arch Pediatr. 2001. PMID: 11270257 Review. French.

10

[The genetics of hereditary cataract].

Beby F, Morle L, Michon L, M B, Edery P, Burillon C, Denis P. Beby F, et al. Among authors: morle l. J Fr Ophtalmol. 2003 Apr;26(4):400-8. J Fr Ophtalmol. 2003. PMID: 12843900 Review. French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

76 results

Search Page

Filters