Mercier B - Search Results

1

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: mercier b. Clin Genet. 2001 Jan;59(1):42-7. doi: 10.1034/j.1399-0004.2001.590107.x. Clin Genet. 2001. PMID: 11168024

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

3

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

4

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

5

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: mercier b. Prenat Diagn. 1993 Dec;13(12):1143-8. doi: 10.1002/pd.1970131210. Prenat Diagn. 1993. PMID: 7513889

6

Association of 1078 del T cystic fibrosis mutation with severe disease.

Moullier P, Jéhanne M, Audrézet MP, Mercier B, Verlingue C, Quéré I, Guillermit H, Raguénès O, Storni V, Rault G, et al. Moullier P, et al. Among authors: mercier b. J Med Genet. 1994 Feb;31(2):159-61. doi: 10.1136/jmg.31.2.159. J Med Genet. 1994. PMID: 7514227 Free PMC article.

7

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: mercier b. Hum Genet. 1994 Jun;93(6):659-62. doi: 10.1007/BF00201566. Hum Genet. 1994. PMID: 7516305

8

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

9

Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->A.

Mercier B, Audrézet MP, Feigelson J, Douchain F, Raguénès O, Verlingue C, Quéré I, Férec C. Mercier B, et al. Hum Mutat. 1994;4(3):224-6. doi: 10.1002/humu.1380040309. Hum Mutat. 1994. PMID: 7530553 No abstract available.

10

Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel alleles.

Verlingue C, Kapranov NI, Mercier B, Ginter EK, Petrova NV, Audrezet MP, Férec C. Verlingue C, et al. Among authors: mercier b. Hum Mutat. 1995;5(3):205-9. doi: 10.1002/humu.1380050304. Hum Mutat. 1995. PMID: 7541273

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