Férec C - Search Results

1

Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR gene.

Bergougnoux A, Délétang K, Pommier A, Varilh J, Houriez F, Altieri JP, Koenig M, Férec C, Claustres M, Lalau G, Bienvenu T, Audrézet MP, Pagin A, Girodon E, Raynal C, Taulan-Cadars M. Bergougnoux A, et al. Among authors: ferec c. J Cyst Fibros. 2019 Jul;18(4):468-475. doi: 10.1016/j.jcf.2018.10.012. Epub 2018 Oct 30. J Cyst Fibros. 2019. PMID: 30389601 Free article.

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

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

6

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

7

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

8

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

9

Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patients.

Audrézet MP, Canki-Klain N, Mercier B, Bracar D, Verlingue C, Férec C. Audrézet MP, et al. Among authors: ferec c. Hum Genet. 1994 Jun;93(6):659-62. doi: 10.1007/BF00201566. Hum Genet. 1994. PMID: 7516305

10

Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.

Mercier B, Verlingue C, Lissens W, Silber SJ, Novelli G, Bonduelle M, Audrézet MP, Férec C. Mercier B, et al. Among authors: ferec c. Am J Hum Genet. 1995 Jan;56(1):272-7. Am J Hum Genet. 1995. PMID: 7529962 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

574 results

Search Page

Filters