C Verlingue
Overview
Explore the profile of C Verlingue including associated specialties, affiliations and a list of published articles.
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Articles
33
Citations
395
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Recent Articles
1.
Amaral M, Pacheco P, Beck S, Farinha C, Penque D, Nogueira P, et al.
J Med Genet
. 2001 Dec;
38(11):777-83.
PMID: 11732487
No abstract available.
2.
Scotet V, De Braekeleer M, Audrezet M, Lode L, Verlingue C, Quere I, et al.
Clin Genet
. 2001 Feb;
59(1):42-7.
PMID: 11168024
Nowadays, most of the neonatal screening programs for cystic fibrosis (CF) combine the assay of immunoreactive trypsinogen (IRT) with the analysis of the most common mutations of the CFTR gene....
3.
Scotet V, De Braekeleer M, Roussey M, Rault G, Parent P, Dagorne M, et al.
Lancet
. 2000 Oct;
356(9232):789-94.
PMID: 11022925
Background: Neonatal screening for cystic fibrosis has been a subject of debate over the past few years. This study assesses 10 years of neonatal screening in Brittany, France, and examines...
4.
Claustres M, Guittard C, Bozon D, Chevalier F, Verlingue C, Ferec C, et al.
Hum Mutat
. 2000 Aug;
16(2):143-56.
PMID: 10923036
We have collated the results of cystic fibrosis (CF) mutation analysis conducted in 19 laboratories in France. We have analyzed 7, 420 CF alleles, demonstrating a total of 310 different...
5.
De Braekeleer M, Mari C, Verlingue C, Allard C, Leblanc J, Simard F, et al.
Clin Genet
. 1998 Apr;
53(1):44-6.
PMID: 9550360
Over the past few years, we have conducted a systematic study of 230 cystic fibrosis (CF) chromosomes in the Saguenay Lac-Saint-Jean (SLSJ) population which has a high CF incidence (1/936...
6.
Verlingue C, Vuillaumier S, Mercier B, Le Gac M, Elion J, Ferec C, et al.
J Med Genet
. 1998 Mar;
35(2):137-40.
PMID: 9507393
This study was aimed at testing if a 5.2 kb untranslated region on both sides of the first CFTR exon, shown to contain regulatory elements, could carry mutations responsible for...
7.
De Braekeleer M, Mari G, Verlingue C, Allard C, Leblanc J, Simard F, et al.
Ann Genet
. 1997 Jan;
40(4):205-8.
PMID: 9526613
We describe the clinical features of six cystic fibrosis (CF) patients from Saguenay Lac-Saint-Jean who bear rare genotypes. Two patients with a delta F508/I148T genotype had pancreatic insufficiency, as did...
8.
Clavel C, PENNAFORTE F, Pigeon F, Verlingue C, Birembaut P, Ferec C
Hum Mutat
. 1997 Jan;
9(4):368-9.
PMID: 9101301
No abstract available.
9.
De Braekeleer M, Chaventre A, Bertorelle G, Verlingue C, Raguenes O, Mercier B, et al.
Hum Genet
. 1996 Aug;
98(2):223-7.
PMID: 8698348
Microsatellite haplotypes were determined for 117 chromosomes carrying the four most frequent mutations in the cystic fibrosis (CF) gene identified in the Breton population of Celtic origin, as well as...
10.
Messaoud T, Verlingue C, Denamur E, Pascaud O, Quere I, Fattoum S, et al.
Eur J Hum Genet
. 1996 Jan;
4(1):20-4.
PMID: 8800923
Cystic fibrosis (CF), the most common lethal genetic disease in the Caucasian population, is caused by mutations in the CF transmembrane conductance regulator gene (CFTR). More than 500 molecular defects...