Fontes M - Search Results

1

The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism.

Hugnot JP, Pedeutour F, Le Calvez C, Grosgeorge J, Passage E, Fontes M, Lazdunski M. Hugnot JP, et al. Among authors: fontes m. Genomics. 1997 Jan 1;39(1):113-6. doi: 10.1006/geno.1996.4450. Genomics. 1997. PMID: 9027495

2

Assignment of a Polycomb-like chromobox gene (CBX2) to human chromosome 17q25.

Gecz J, Gaunt SJ, Passage E, Burton RD, Cudrey C, Pearce JJ, Fontes M. Gecz J, et al. Among authors: fontes m. Genomics. 1995 Mar 1;26(1):130-3. doi: 10.1016/0888-7543(95)80091-y. Genomics. 1995. PMID: 7782071

3

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. Among authors: fontes m. Genomics. 1993 Jan;15(1):243-5. doi: 10.1006/geno.1993.1051. Genomics. 1993. PMID: 8432548 No abstract available.

4

Use of interspersed repetitive sequences-PCR products for cDNA selection.

Villard L, Passage E, Colleaux L, Fontes M. Villard L, et al. Among authors: fontes m. Mamm Genome. 1995 Sep;6(9):617-22. doi: 10.1007/BF00352368. Mamm Genome. 1995. PMID: 8535069

5

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: fontes m. 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.

6

Molecular dissection of the Schwann cell specific promoter of the PMP22 gene.

Sabéran-Djoneidi D, Sanguedolce V, Assouline Z, Lévy N, Passage E, Fontés M. Sabéran-Djoneidi D, et al. Among authors: fontes m. Gene. 2000 May 2;248(1-2):223-31. doi: 10.1016/s0378-1119(00)00116-5. Gene. 2000. PMID: 10806367

7

Isolation and regional mapping of cDNAs expressed during early human development.

Jay P, Diriong S, Taviaux S, Roeckel N, Mattéi MG, Audit M, Bergé-Lefranc JL, Fontès M, Berta P. Jay P, et al. Among authors: fontes m. Genomics. 1997 Jan 1;39(1):104-8. doi: 10.1006/geno.1996.4470. Genomics. 1997. PMID: 9027493

8

Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?

Briault S, Villard L, Rogner U, Coy J, Odent S, Lucas J, Passage E, Zhu D, Shrimpton A, Pembrey M, Till M, Guichet A, Dessay S, Fontes M, Poustka A, Moraine C. Briault S, et al. Among authors: fontes m. Am J Med Genet. 2000 Nov 13;95(2):178-81. doi: 10.1002/1096-8628(20001113)95:2<178::aid-ajmg17>3.0.co;2-v. Am J Med Genet. 2000. PMID: 11078572

9

Behavioural profiling of a murine Charcot-Marie-Tooth disease type 1A model.

Norreel JC, Jamon M, Riviere G, Passage E, Fontes M, Clarac F. Norreel JC, et al. Among authors: fontes m. Eur J Neurosci. 2001 Apr;13(8):1625-34. doi: 10.1046/j.0953-816x.2001.01535.x. Eur J Neurosci. 2001. PMID: 11328356

10

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.

Huxley C, Passage E, Manson A, Putzu G, Figarella-Branger D, Pellissier JF, Fontés M. Huxley C, et al. Among authors: fontes m. Hum Mol Genet. 1996 May;5(5):563-9. doi: 10.1093/hmg/5.5.563. Hum Mol Genet. 1996. PMID: 8733121

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