Mercier B - Search Results

1

CFTR mutations in the Algerian population.

Loumi O, Ferec C, Mercier B, Creff J, Fercot B, Denine R, Grangaud JP. Loumi O, et al. Among authors: mercier b. J Cyst Fibros. 2008 Jan;7(1):54-9. doi: 10.1016/j.jcf.2007.04.004. Epub 2007 Jun 14. J Cyst Fibros. 2008. PMID: 17572159 Free article.

2

Identification of six novel mutations in the CFTR gene of patients from Bulgaria by screening the twenty seven exons and exon/intron boundaries using DGGE and direct DNA sequencing.

Savov A, Mercier B, Kalaydjieva L, Férec C. Savov A, et al. Among authors: mercier b. Hum Mol Genet. 1994 Jan;3(1):57-60. doi: 10.1093/hmg/3.1.57. Hum Mol Genet. 1994. PMID: 7512860

3

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

4

Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patients.

Férec C, Novelli G, Verlingue C, Quéré I, Dallapiccola B, Audrézet MP, Mercier B. Férec C, et al. Among authors: mercier b. Mol Cell Probes. 1995 Apr;9(2):135-7. doi: 10.1016/s0890-8508(95)80038-7. Mol Cell Probes. 1995. PMID: 7541510

5

A novel mutation in exon 3 of the CFTR gene.

Guillermit H, Jéhanne M, Quéré I, Audrézet MP, Mercier B, Férec C. Guillermit H, et al. Among authors: mercier b. Hum Genet. 1993 Apr;91(3):233-5. doi: 10.1007/BF00218262. Hum Genet. 1993. PMID: 7682984

6

Identification of 12 novel mutations in the CFTR gene.

Audrézet MP, Mercier B, Guillermit H, Quéré I, Verlingue C, Rault G, Férec C. Audrézet MP, et al. Among authors: mercier b. Hum Mol Genet. 1993 Jan;2(1):51-4. doi: 10.1093/hmg/2.1.51. Hum Mol Genet. 1993. PMID: 7683952

7

Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany.

De Braekeleer M, Chaventré A, Bertorelle G, Verlingue C, Raguénès O, Mercier B, Férec C. De Braekeleer M, et al. Among authors: mercier b. Hum Genet. 1996 Aug;98(2):223-7. doi: 10.1007/s004390050196. Hum Genet. 1996. PMID: 8698348

8

Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR gene.

Macek M Jr, Mercier B, Macková A, Miller PW, Hamosh A, Férec C, Cutting GR. Macek M Jr, et al. Among authors: mercier b. Hum Mutat. 1997;9(2):136-47. doi: 10.1002/(SICI)1098-1004(1997)9:2<136::AID-HUMU6>3.0.CO;2-7. Hum Mutat. 1997. PMID: 9067754

9

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

10

Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients.

Verlingue C, Vuillaumier S, Mercier B, Le Gac M, Elion J, Férec C, Denamur E. Verlingue C, et al. Among authors: mercier b. J Med Genet. 1998 Feb;35(2):137-40. doi: 10.1136/jmg.35.2.137. J Med Genet. 1998. PMID: 9507393 Free PMC article.

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