Weissenbach J - Search Results

1

Exclusion of genes coding for proteins of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach.

Dufour C, Carrier L, Hengstenberg C, Bercovici J, Dausse E, Weissenbach J, Dubourg O, Komajda M, Schwartz K, Beckmann JS. Dufour C, et al. Among authors: weissenbach j. C R Acad Sci III. 1993;316(5):474-81. C R Acad Sci III. 1993. PMID: 8221230

2

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.

Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, Labeit S, James M, Beckmann J, Weissenbach J, Vosberg HP, Fiszman M, Komajda M, Schwartz K. Bonne G, et al. Among authors: weissenbach j. Nat Genet. 1995 Dec;11(4):438-40. doi: 10.1038/ng1295-438. Nat Genet. 1995. PMID: 7493026

3

Readjusting the localization of long QT syndrome gene on chromosome 11p15.

Dausse E, Denjoy I, Kahlem P, Bennaceur M, Fauré S, Weissenbach J, Coumel P, Schwartz K, Guicheney P. Dausse E, et al. Among authors: weissenbach j. C R Acad Sci III. 1995 Aug;318(8):879-85. C R Acad Sci III. 1995. PMID: 7583778

4

The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.

Stevanin G, Cancel G, Dürr A, Chneiweiss H, Dubourg O, Weissenbach J, Cann HM, Agid Y, Brice A. Stevanin G, et al. Among authors: weissenbach j. Am J Hum Genet. 1995 Jan;56(1):193-201. Am J Hum Genet. 1995. PMID: 7825578 Free PMC article.

5

The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q.

Stevanin G, Sousa PS, Cancel G, Dürr A, Dubourg O, Nicholson GA, Weissenbach J, Jardim E, Agid Y, Cassa E, et al. Stevanin G, et al. Among authors: weissenbach j. Neurobiol Dis. 1994 Nov;1(1-2):79-82. doi: 10.1006/nbdi.1994.0010. Neurobiol Dis. 1994. PMID: 9216989

6

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.

Helbling-Leclerc A, Zhang X, Topaloglu H, Cruaud C, Tesson F, Weissenbach J, Tomé FM, Schwartz K, Fardeau M, Tryggvason K, et al. Helbling-Leclerc A, et al. Among authors: weissenbach j. Nat Genet. 1995 Oct;11(2):216-8. doi: 10.1038/ng1095-216. Nat Genet. 1995. PMID: 7550355

7

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

8

Exclusion of HRAS from long QT locus.

Roy N, Kahlem P, Dausse E, Bennaceur M, Fauré S, Weissenbach J, Komajda M, Denjoy I, Coumel P, Schwartz K, et al. Roy N, et al. Among authors: weissenbach j. Nat Genet. 1994 Oct;8(2):113-4. doi: 10.1038/ng1094-113. Nat Genet. 1994. PMID: 7842005 No abstract available.

9

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

Medhioub M, Cherif D, Benessy F, Silbermann F, Gubler MC, Le Paslier D, Cohen D, Weissenbach J, Beckmann J, Antignac C. Medhioub M, et al. Among authors: weissenbach j. Genomics. 1994 Jul 15;22(2):296-301. doi: 10.1006/geno.1994.1387. Genomics. 1994. PMID: 7806215

10

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12.

Azibi K, Bachner L, Beckmann JS, Matsumura K, Hamouda E, Chaouch M, Chaouch A, Ait-Ouarab R, Vignal A, Weissenbach J, et al. Azibi K, et al. Among authors: weissenbach j. Hum Mol Genet. 1993 Sep;2(9):1423-8. doi: 10.1093/hmg/2.9.1423. Hum Mol Genet. 1993. PMID: 8242065

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