Audrezet MP - Search Results

1

Ferec C, Giroux MA, Audrezet MP, Robaszkiewicz M. Ferec C, et al. Among authors: audrezet mp. Pathol Biol (Paris). 1997 Dec;45(10):871-5. Pathol Biol (Paris). 1997. PMID: 9769951 Review.

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. Among authors: audrezet mp. 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. 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: audrezet mp. 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. Among authors: audrezet mp. 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. Among authors: audrezet mp. 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: audrezet mp. 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: audrezet mp. 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. 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: audrezet mp. Am J Hum Genet. 1995 Jan;56(1):272-7. Am J Hum Genet. 1995. PMID: 7529962 Free PMC article.

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