Ferec C - Search Results

1

A 3' splice site consensus sequence mutation in the cystic fibrosis gene.

Guillermit H, Fanen P, Ferec C. Guillermit H, et al. Among authors: ferec c. Hum Genet. 1990 Sep;85(4):450-3. doi: 10.1007/BF02428306. Hum Genet. 1990. PMID: 2210769

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

3

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G, et al. Dörk T, et al. Among authors: ferec c. Hum Genet. 1992 Feb;88(4):417-25. doi: 10.1007/BF00215676. Hum Genet. 1992. PMID: 1371263

4

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. Among authors: ferec c. 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.

5

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: ferec c. 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.

6

[Gene mutations of cystic fibrosis in Brittany population].

Ferec C, Guillermit H, Chaventre A. Ferec C, et al. Pathol Biol (Paris). 1991 Jun;39(6):577-80. Pathol Biol (Paris). 1991. PMID: 1923586 French.

7

Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French population.

Vidaud M, Ferec C, Attree O, Pascal O, Guillermit H, Ghanem N, Martin J, Moisan JP, Feingold J, Goossens M. Vidaud M, et al. Among authors: ferec c. Hum Genet. 1990 Sep;85(4):434-5. doi: 10.1007/BF02428302. Hum Genet. 1990. PMID: 1976598

8

[Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene].

Férec C, Guillermit H, Verlingue C, Parent P, Puissant H, Jehanne M, Saleun JP. Férec C, et al. Arch Fr Pediatr. 1990 Aug-Sep;47(7):507-10. Arch Fr Pediatr. 1990. PMID: 2256790 French.

9

Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population.

Vidaud M, Kitzis A, Ferec C, Bozon D, Dumur V, Giraud G, David F, Pascal O, Auvinet M, Morel Y, et al. Vidaud M, et al. Among authors: ferec c. Hum Genet. 1989 Jan;81(2):183-4. doi: 10.1007/BF00293899. Hum Genet. 1989. PMID: 2563252

10

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

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

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