Vignal A - Search Results

1

Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome.

Edery P, Manach Y, Le Merrer M, Till M, Vignal A, Lyonnet S, Munnich A. Edery P, et al. Among authors: vignal a. Am J Med Genet. 1994 Aug 15;52(2):174-7. doi: 10.1002/ajmg.1320520210. Am J Med Genet. 1994. PMID: 7802004

2

Assignment of microsatellite sequences to the region duplicated in CMT1A (17p12): a useful tool for diagnosis.

Cudrey C, Chevillard C, Le Paslier D, Vignal A, Passage E, Fontes M. Cudrey C, et al. Among authors: vignal a. J Med Genet. 1995 Mar;32(3):231-3. doi: 10.1136/jmg.32.3.231. J Med Genet. 1995. PMID: 7783177 Free PMC article.

3

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: vignal a. Hum Mol Genet. 1993 Sep;2(9):1423-8. doi: 10.1093/hmg/2.9.1423. Hum Mol Genet. 1993. PMID: 8242065

4

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping.

Ben Hamida C, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D, et al. Ben Hamida C, et al. Among authors: vignal a. Nat Genet. 1993 Oct;5(2):195-200. doi: 10.1038/ng1093-195. Nat Genet. 1993. PMID: 8252047

5

A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.

Stevanin G, Le Guern E, Ravisé N, Chneiweiss H, Dürr A, Cancel G, Vignal A, Boch AL, Ruberg M, Penet C, et al. Stevanin G, et al. Among authors: vignal a. Am J Hum Genet. 1994 Jan;54(1):11-20. Am J Hum Genet. 1994. PMID: 8279460 Free PMC article.

6

A radiation hybrid map of 506 STS markers spanning human chromosome 11.

James MR, Richard CW 3rd, Schott JJ, Yousry C, Clark K, Bell J, Terwilliger JD, Hazan J, Dubay C, Vignal A, et al. James MR, et al. Among authors: vignal a. Nat Genet. 1994 Sep;8(1):70-6. doi: 10.1038/ng0994-70. Nat Genet. 1994. PMID: 7987395

7

Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the gene.

Le Guern E, Ravise N, Gugenheim M, Vignal A, Penet C, Bouche P, Weissenbach J, Agid Y, Brice A. Le Guern E, et al. Among authors: vignal a. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):463-9. doi: 10.1016/0960-8966(94)90085-x. Neuromuscul Disord. 1994. PMID: 7881290

8

Physical mapping of 30 CA repeats on human chromosome 22.

Demczuk S, Delattre O, Vignal A, Weissenbach J, Thomas G, Aurias A. Demczuk S, et al. Among authors: vignal a. Genomics. 1995 May 20;27(2):345-7. doi: 10.1006/geno.1995.1053. Genomics. 1995. PMID: 7558003

9

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: vignal a. Nat Genet. 1994 Jun;7(2 Spec No):246-339. doi: 10.1038/ng0694supp-246. Nat Genet. 1994. PMID: 7545953

10

A second-generation linkage map of the human genome.

Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M. Weissenbach J, et al. Among authors: vignal a. Nature. 1992 Oct 29;359(6398):794-801. doi: 10.1038/359794a0. Nature. 1992. PMID: 1436057

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