Fontès M - Search Results

1

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

2

A limited genomic region contains the human REG and REG-related genes.

Bartoli C, Dagorn JC, Fontes M, Bergé-Lefranc JL. Bartoli C, et al. Among authors: fontes m. Eur J Hum Genet. 1995;3(6):344-50. doi: 10.1159/000472323. Eur J Hum Genet. 1995. PMID: 8825576

3

Characterization of the human jumonji gene.

Bergé-Lefranc JL, Jay P, Massacrier A, Cau P, Mattei MG, Bauer S, Marsollier C, Berta P, Fontes M. Bergé-Lefranc JL, et al. Among authors: fontes m. Hum Mol Genet. 1996 Oct;5(10):1637-41. doi: 10.1093/hmg/5.10.1637. Hum Mol Genet. 1996. PMID: 8894700

4

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.

5

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. Among authors: fontes m. Mamm Genome. 1993;4(2):124-6. doi: 10.1007/BF00290438. Mamm Genome. 1993. PMID: 8431637 No abstract available.

6

Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome.

Moncla A, Piras L, Arbex OF, Muscatelli F, Mattei MG, Mattei JF, Fontes M. Moncla A, et al. Among authors: fontes m. Hum Genet. 1993 Feb;90(6):657-60. doi: 10.1007/BF00202487. Hum Genet. 1993. PMID: 8444473

7

Physical mapping of an Xq-proximal interstitial duplication in a male.

Muscatelli F, Verna JM, Philip N, Moncla A, Mattei MG, Mattei JF, Fontes M. Muscatelli F, et al. Among authors: fontes m. Hum Genet. 1992 Mar;88(6):691-4. doi: 10.1007/BF02265299. Hum Genet. 1992. PMID: 1551675

8

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

9

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

10

ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein.

Cardoso C, Lutz Y, Mignon C, Compe E, Depetris D, Mattei MG, Fontes M, Colleaux L. Cardoso C, et al. Among authors: fontes m. J Med Genet. 2000 Oct;37(10):746-51. doi: 10.1136/jmg.37.10.746. J Med Genet. 2000. PMID: 11015451 Free PMC article.

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