Chevillard C - Search Results

1

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility.

Machev N, Saut N, Longepied G, Terriou P, Navarro A, Levy N, Guichaoua M, Metzler-Guillemain C, Collignon P, Frances AM, Belougne J, Clemente E, Chiaroni J, Chevillard C, Durand C, Ducourneau A, Pech N, McElreavey K, Mattei MG, Mitchell MJ. Machev N, et al. Among authors: chevillard c. J Med Genet. 2004 Nov;41(11):814-25. doi: 10.1136/jmg.2004.022111. J Med Genet. 2004. PMID: 15520406 Free PMC article.

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: chevillard c. 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

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome.

Chevillard C, Le Paslier D, Passage E, Ougen P, Billault A, Boyer S, Mazan S, Bachellerie JP, Vignal A, Cohen D, et al. Chevillard C, et al. Hum Mol Genet. 1993 Aug;2(8):1235-43. doi: 10.1093/hmg/2.8.1235. Hum Mol Genet. 1993. PMID: 8401506

4

Chromosomal localization of human homologs of the Drosophila heterochromatin protein 1 (HP1) gene.

Chevillard C, Reik W, McDermott M, Fontes M, Mattei MG, Singh PB. Chevillard C, et al. Mamm Genome. 1993;4(2):124-6. doi: 10.1007/BF00290438. Mamm Genome. 1993. PMID: 8431637 No abstract available.

5

Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridization.

Chevillard C, Attali B, Lesage F, Fontes M, Barhanin J, Lazdunski M, Mattei MG. Chevillard C, et al. Genomics. 1993 Jan;15(1):243-5. doi: 10.1006/geno.1993.1051. Genomics. 1993. PMID: 8432548 No abstract available.

6

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.

Villard L, Lévy N, Xiang F, Kpebe A, Labelle V, Chevillard C, Zhang Z, Schwartz CE, Tardieu M, Chelly J, Anvret M, Fontès M. Villard L, et al. Among authors: chevillard c. J Med Genet. 2001 Jul;38(7):435-42. doi: 10.1136/jmg.38.7.435. J Med Genet. 2001. PMID: 11432961 Free PMC article.

7

Genetics of parasitic infections.

Dessein AJ, Chevillard C, Marquet S, Henri S, Hillaire D, Dessein H. Dessein AJ, et al. Among authors: chevillard c. Drug Metab Dispos. 2001 Apr;29(4 Pt 2):484-8. Drug Metab Dispos. 2001. PMID: 11259337

8

IL13RA2 gene polymorphisms are associated with systemic sclerosis.

Granel B, Allanore Y, Chevillard C, Arnaud V, Marquet S, Weiller PJ, Durand JM, Harlé JR, Grange C, Frances Y, Berbis P, Gaudart J, de Micco P, Kahan A, Dessein A. Granel B, et al. Among authors: chevillard c. J Rheumatol. 2006 Oct;33(10):2015-9. Epub 2006 Sep 15. J Rheumatol. 2006. PMID: 16981293

9

A STAT6 gene polymorphism is associated with high infection levels in urinary schistosomiasis.

He H, Isnard A, Kouriba B, Cabantous S, Dessein A, Doumbo O, Chevillard C. He H, et al. Among authors: chevillard c. Genes Immun. 2008 Apr;9(3):195-206. doi: 10.1038/gene.2008.2. Epub 2008 Feb 14. Genes Immun. 2008. PMID: 18273035

10

A functional promoter variant in IL12B predisposes to cerebral malaria.

Marquet S, Doumbo O, Cabantous S, Poudiougou B, Argiro L, Safeukui I, Konate S, Sissoko S, Chevereau E, Traore A, Keita MM, Chevillard C, Abel L, Dessein AJ. Marquet S, et al. Among authors: chevillard c. Hum Mol Genet. 2008 Jul 15;17(14):2190-5. doi: 10.1093/hmg/ddn118. Epub 2008 Apr 15. Hum Mol Genet. 2008. PMID: 18413324

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