Beckmann JS - Search Results

1

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. Among authors: beckmann js. Hum Mol Genet. 1992 Nov;1(8):621-4. doi: 10.1093/hmg/1.8.621. Hum Mol Genet. 1992. PMID: 1363783

2

Mapping of two chromosome 15 microsatellites.

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

3

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: beckmann js. Hum Mol Genet. 1995 Apr;4(4):717-25. doi: 10.1093/hmg/4.4.717. Hum Mol Genet. 1995. PMID: 7633422

4

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: beckmann js. Hum Mol Genet. 1995 Mar;4(3):459-63. doi: 10.1093/hmg/4.3.459. Hum Mol Genet. 1995. PMID: 7795603

5

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. Hum Mol Genet. 1993 Dec;2(12):2019-30. doi: 10.1093/hmg/2.12.2019. Hum Mol Genet. 1993. PMID: 7906587

6

Dinucleotide repeat at the D15S129 locus.

Richard I, Bourg N, Beckmann JS. Richard I, et al. Among authors: beckmann js. Hum Mol Genet. 1993 Dec;2(12):2199. doi: 10.1093/hmg/2.12.2199-a. Hum Mol Genet. 1993. PMID: 8111397 No abstract available.

7

Dinucleotide repeat polymorphism at the locus D15S222.

Fougerousse F, Pasturaud P, Beckmann JS. Fougerousse F, et al. Among authors: beckmann js. Hum Mol Genet. 1993 Dec;2(12):2200. doi: 10.1093/hmg/2.12.2200. Hum Mol Genet. 1993. PMID: 8111400 No abstract available.

8

The gene for creatine kinase, mitochondrial 2 (sarcomeric; CKMT2), maps to chromosome 5q13.3.

Richard I, Devaud C, Cherif D, Cohen D, Beckmann JS. Richard I, et al. Among authors: beckmann js. Genomics. 1993 Oct;18(1):134-6. doi: 10.1006/geno.1993.1437. Genomics. 1993. PMID: 8276398

9

An STS map of the limb girdle muscular dystrophy type 2A region.

Richard I, Roudaut C, Fougerousse F, Chiannilkulchai N, Beckmann JS. Richard I, et al. Among authors: beckmann js. Mamm Genome. 1995 Oct;6(10):754-6. doi: 10.1007/BF00354303. Mamm Genome. 1995. PMID: 8563179 No abstract available.

10

Molecular cloning of mouse canp3, the gene associated with limb-girdle muscular dystrophy 2A in human.

Richard I, Beckmann JS. Richard I, et al. Among authors: beckmann js. Mamm Genome. 1996 May;7(5):377-9. doi: 10.1007/s003359900108. Mamm Genome. 1996. PMID: 8661728 No abstract available.

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