Richard I - Search Results

1

A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.

Dinçer P, Akçören Z, Demir E, Richard I, Sancak O, Kale G, Ozme S, Karaduman A, Tan E, Urtizberea JA, Beckmann JS, Topaloğlu H. Dinçer P, et al. Among authors: richard i. J Med Genet. 2000 May;37(5):361-7. doi: 10.1136/jmg.37.5.361. J Med Genet. 2000. PMID: 10807695 Free PMC article.

2

Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy.

Richard I, Broux O, Hillaire D, Cherif D, Fougerousse F, Cohen D, Beckmann JS. Richard I, et al. Hum Mol Genet. 1992 Nov;1(8):621-4. doi: 10.1093/hmg/1.8.621. Hum Mol Genet. 1992. PMID: 1363783

3

Mapping of two chromosome 15 microsatellites.

Fougerousse F, Richard I, Broux O, Cohen D, Beckmann JS. Fougerousse F, et al. Among authors: richard i. Genomics. 1992 Jul;13(3):903-4. doi: 10.1016/0888-7543(92)90184-t. Genomics. 1992. PMID: 1639425 No abstract available.

4

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.

Beckmann JS, Richard I, Hillaire D, Broux O, Antignac C, Bois E, Cann H, Cottingham RW Jr, Feingold N, Feingold J, et al. Beckmann JS, et al. Among authors: richard i. C R Acad Sci III. 1991;312(4):141-8. C R Acad Sci III. 1991. PMID: 1901754

5

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.

Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C, et al. Lim LE, et al. Among authors: richard i. Nat Genet. 1995 Nov;11(3):257-65. doi: 10.1038/ng1195-257. Nat Genet. 1995. PMID: 7581448

6

A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.

Chiannilkulchai N, Pasturaud P, Richard I, Auffray C, Beckmann JS. Chiannilkulchai N, et al. Among authors: richard i. Hum Mol Genet. 1995 Apr;4(4):717-25. doi: 10.1093/hmg/4.4.717. Hum Mol Genet. 1995. PMID: 7633422

7

How neutral are synonymous codon mutations?

Richard I, Beckmann JS. Richard I, et al. Nat Genet. 1995 Jul;10(3):259. doi: 10.1038/ng0795-259. Nat Genet. 1995. PMID: 7670461 No abstract available.

8

Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus.

Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Allamand V, et al. Among authors: richard i. Hum Mol Genet. 1995 Mar;4(3):459-63. doi: 10.1093/hmg/4.3.459. Hum Mol Genet. 1995. PMID: 7795603

9

The EUROGEM map of human chromosome 15.

Joyce C, Fanning L, Malcolm S, Richard I, Broux O, Beckmann JS, Flint T, Kruse TA, Vergnaud G, Cox SA, et al. Joyce C, et al. Among authors: richard i. Eur J Hum Genet. 1994;2(3):232-3. Eur J Hum Genet. 1994. PMID: 7834295 No abstract available.

10

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites.

Beckmann JS, Tomfohrde J, Barnes RI, Williams M, Broux O, Richard I, Weissenbach J, Bowcock AM. Beckmann JS, et al. Among authors: richard i. Hum Mol Genet. 1993 Dec;2(12):2019-30. doi: 10.1093/hmg/2.12.2019. Hum Mol Genet. 1993. PMID: 7906587

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