Férec C - Search Results

1

Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?

Scotet V, Audrézet MP, Roussey M, Rault G, Dirou-Prigent A, Journel H, Moisan-Petit V, Storni V, Férec C. Scotet V, et al. Among authors: ferec c. Pediatrics. 2006 Nov;118(5):e1523-9. doi: 10.1542/peds.2005-3161. Epub 2006 Oct 2. Pediatrics. 2006. PMID: 17015492

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 mutation in exon 7 of the CFTR gene is common in the western part of France.

Audrezet MP, Mercier B, Guillermit H, Ferec C. Audrezet MP, et al. Among authors: ferec c. J Med Genet. 1992 Sep;29(9):679. doi: 10.1136/jmg.29.9.679-a. J Med Genet. 1992. PMID: 1404304 Free PMC article. No abstract available.

4

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.

5

A 3' splice site consensus sequence mutation in the cystic fibrosis gene.

Guillermit H, Fanen P, Ferec C. Guillermit H, et al. Among authors: ferec c. Hum Genet. 1990 Sep;85(4):450-3. doi: 10.1007/BF02428306. Hum Genet. 1990. PMID: 2210769

6

[Approaching the gene of mucoviscidosis. New data].

Ferec C, Morin JF, Parent P, Jehanne M, Chabaud JJ, Gouedard G, Journel H, Saleun JP. Ferec C, et al. Arch Fr Pediatr. 1988 Oct;45(8):531-5. Arch Fr Pediatr. 1988. PMID: 3214245 French.

7

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

8

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

9

Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosis.

Verlingue C, Mercier B, Lecoq I, Audrézet MP, Laroche D, Travert G, Férec C. Verlingue C, et al. Among authors: ferec c. Hum Genet. 1994 Apr;93(4):429-34. doi: 10.1007/BF00201669. Hum Genet. 1994. PMID: 7513292

10

Asymptomatic carrier of two CFTR mutations: consequences for prenatal diagnosis?

Verlingue C, David A, Audrezet MP, Le Roux MG, Mercier B, Moisan JP, Ferec C. Verlingue C, et al. Among authors: ferec c. Prenat Diagn. 1993 Dec;13(12):1143-8. doi: 10.1002/pd.1970131210. Prenat Diagn. 1993. PMID: 7513889

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