Ferec C - Search Results

1

Identification of a novel pancreatitis-associated missense mutation, R116C, in the human cationic trypsinogen gene (PRSS1).

Le Maréchal C, Bretagne JF, Raguénès O, Quéré I, Chen JM, Ferec C. Le Maréchal C, et al. Among authors: ferec c. Mol Genet Metab. 2001 Nov;74(3):342-4. doi: 10.1006/mgme.2001.3246. Mol Genet Metab. 2001. PMID: 11708864

2

Detection of over 98% cystic fibrosis mutations in a Celtic population.

Férec C, Audrezet MP, Mercier B, Guillermit H, Moullier P, Quere I, Verlingue C. Férec C, et al. Nat Genet. 1992 Jun;1(3):188-91. doi: 10.1038/ng0692-188. Nat Genet. 1992. PMID: 1284639

3

A polymorphism in intron 20 of the CFTR gene.

Quere I, Guillermit H, Mercier B, Audrezet MP, Ferec C. Quere I, et al. Among authors: ferec c. Nucleic Acids Res. 1991 Oct 11;19(19):5453. doi: 10.1093/nar/19.19.5453-a. Nucleic Acids Res. 1991. PMID: 1717950 Free PMC article.

4

Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresis.

Férec C, Verlingue C, Audrézet MP, Guillermit H, Quéré I, Raguenes O, Mercier B. Férec C, et al. Fetal Diagn Ther. 1993 Sep-Oct;8(5):341-50. doi: 10.1159/000263850. Fetal Diagn Ther. 1993. PMID: 7505587

5

Genotype analysis of adult cystic fibrosis patients.

Férec C, Verlingue C, Guillermit H, Quéré I, Raguénès O, Feigelson J, Audrézet MP, Moullier P, Mercier B. Férec C, et al. Hum Mol Genet. 1993 Oct;2(10):1557-60. doi: 10.1093/hmg/2.10.1557. Hum Mol Genet. 1993. PMID: 7505690

6

Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->A.

Mercier B, Audrézet MP, Feigelson J, Douchain F, Raguénès O, Verlingue C, Quéré I, Férec C. Mercier B, et al. Among authors: ferec c. Hum Mutat. 1994;4(3):224-6. doi: 10.1002/humu.1380040309. Hum Mutat. 1994. PMID: 7530553 No abstract available.

7

Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patients.

Férec C, Novelli G, Verlingue C, Quéré I, Dallapiccola B, Audrézet MP, Mercier B. Férec C, et al. Mol Cell Probes. 1995 Apr;9(2):135-7. doi: 10.1016/s0890-8508(95)80038-7. Mol Cell Probes. 1995. PMID: 7541510

8

Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delT.

Mercier B, Lissens W, Audrézet MP, Bonduelle M, Quéré I, Hilbert P, Liebaers I, Férec C. Mercier B, et al. Among authors: ferec c. Hum Mutat. 1995;6(2):188-9. doi: 10.1002/humu.1380060215. Hum Mutat. 1995. PMID: 7581406 No abstract available.

9

HLA class II typing and idiopathic IgA nephropathy (IgAN): DQB1*0301, a possible marker of unfavorable outcome.

Raguénès O, Mercier B, Clèdes J, Whebe B, Férec C. Raguénès O, et al. Among authors: ferec c. Tissue Antigens. 1995 Apr;45(4):246-9. doi: 10.1111/j.1399-0039.1995.tb02447.x. Tissue Antigens. 1995. PMID: 7638860

10

A novel mutation in exon 3 of the CFTR gene.

Guillermit H, Jéhanne M, Quéré I, Audrézet MP, Mercier B, Férec C. Guillermit H, et al. Among authors: ferec c. Hum Genet. 1993 Apr;91(3):233-5. doi: 10.1007/BF00218262. Hum Genet. 1993. PMID: 7682984

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