Verlingue C - Search Results

1

Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis.

Scotet V, de Braekeleer M, Roussey M, Rault G, Parent P, Dagorne M, Journel H, Lemoigne A, Codet JP, Catheline M, David V, Chaventré A, Duguépéroux I, Verlingue C, Quéré I, Mercier B, Audrézet MP, Férec C. Scotet V, et al. Among authors: verlingue c. Lancet. 2000 Sep 2;356(9232):789-94. doi: 10.1016/S0140-6736(00)02652-0. Lancet. 2000. PMID: 11022925

2

[Cystic fibrosis gene mutations in the West of France: clinical application].

Verlingue C, Travert G, Le Roux MG, Laroche D, Audrézet MP, Mercier B, Moisan JP, Férec C. Verlingue C, et al. Ann Biol Clin (Paris). 1994;52(11):757-64. Ann Biol Clin (Paris). 1994. PMID: 7747883 French.

3

Screening for cystic fibrosis in dried blood spots of newborns.

Audrézet MP, Costes B, Ghanem N, Fanen P, Verlingue C, Morin JF, Mercier B, Goossens M, Férec C. Audrézet MP, et al. Among authors: verlingue c. Mol Cell Probes. 1993 Dec;7(6):497-502. doi: 10.1006/mcpr.1993.1073. Mol Cell Probes. 1993. PMID: 8145780

4

Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses.

Férec C, Verlingue C, Parent P, Morin JF, Codet JP, Rault G, Dagorne M, Lemoigne A, Journel H, Roussey M, et al. Férec C, et al. Among authors: verlingue c. Hum Genet. 1995 Nov;96(5):542-8. doi: 10.1007/BF00197409. Hum Genet. 1995. PMID: 8530001

5

Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis.

Scotet V, De Braekeleer M, Audrézet MP, Lodé L, Verlingue C, Quéré I, Mercier B, Duguépéroux I, Codet JP, Moineau MP, Parent P, Férec C. Scotet V, et al. Among authors: verlingue c. Clin Genet. 2001 Jan;59(1):42-7. doi: 10.1034/j.1399-0004.2001.590107.x. Clin Genet. 2001. PMID: 11168024

6

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: verlingue c. Nat Genet. 1992 Jun;1(3):188-91. doi: 10.1038/ng0692-188. Nat Genet. 1992. PMID: 1284639

7

[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis].

Ferec C, Verlingue C, Parent P. Ferec C, et al. Among authors: verlingue c. J Genet Hum. 1989 Dec;37(4-5):407-23. J Genet Hum. 1989. PMID: 2635718 French.

8

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: verlingue c. Fetal Diagn Ther. 1993 Sep-Oct;8(5):341-50. doi: 10.1159/000263850. Fetal Diagn Ther. 1993. PMID: 7505587

9

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: verlingue c. Hum Mol Genet. 1993 Oct;2(10):1557-60. doi: 10.1093/hmg/2.10.1557. Hum Mol Genet. 1993. PMID: 7505690

10

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. Hum Genet. 1994 Apr;93(4):429-34. doi: 10.1007/BF00201669. Hum Genet. 1994. PMID: 7513292

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