Weissenbach J - Search Results

1

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

2

Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.

Bowcock AM, Tomfohrde J, Weissenbach J, Bonne-Tamir B, St George-Hyslop P, Giagheddu M, Cavalli-Sforza LL, Farrer LA. Bowcock AM, et al. Among authors: weissenbach j. Am J Hum Genet. 1994 Jan;54(1):79-87. Am J Hum Genet. 1994. PMID: 8279473 Free PMC article.

3

A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus.

White A, Tomfohrde J, Stewart E, Barnes R, Le Paslier D, Weissenbach J, Cavalli-Sforza L, Farrer L, Bowcock A. White A, et al. Among authors: weissenbach j. Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):10105-9. doi: 10.1073/pnas.90.21.10105. Proc Natl Acad Sci U S A. 1993. PMID: 8234264 Free PMC article.

4

The 1993-94 Généthon human genetic linkage map.

Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J. Gyapay G, et al. Among authors: weissenbach j. Nat Genet. 1994 Jun;7(2 Spec No):246-339. doi: 10.1038/ng0694supp-246. Nat Genet. 1994. PMID: 7545953

5

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

6

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families.

Passos-Bueno MR, Richard I, Vainzof M, Fougerousse F, Weissenbach J, Broux O, Cohen D, Akiyama J, Marie SK, Carvalho AA, et al. Passos-Bueno MR, et al. Among authors: weissenbach j. J Med Genet. 1993 May;30(5):385-7. doi: 10.1136/jmg.30.5.385. J Med Genet. 1993. PMID: 8320700 Free PMC article.

7

A first high-density map of 981 biallelic markers on human chromosome 14.

Escary JL, Bottius E, Prince N, Reyes C, Fiawoumo Y, Caloustian C, Bruls T, Fujiyama A, Cooper RS, Adeyemo AA, Lathrop GM, Weissenbach J, Gyapay G, Foglio M, Beckmann JS. Escary JL, et al. Among authors: weissenbach j. Genomics. 2000 Dec 1;70(2):153-64. doi: 10.1006/geno.2000.6369. Genomics. 2000. PMID: 11112343

8

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

9

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

10

High-density genetic map of the BRCA1 region of chromosome 17q12-q21.

Anderson LA, Friedman L, Osborne-Lawrence S, Lynch E, Weissenbach J, Bowcock A, King MC. Anderson LA, et al. Among authors: weissenbach j. Genomics. 1993 Sep;17(3):618-23. doi: 10.1006/geno.1993.1381. Genomics. 1993. PMID: 8244378

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