Férec C - Search Results

1

Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.

De Braekeleer M, Férec C. De Braekeleer M, et al. Among authors: ferec c. Mol Hum Reprod. 1996 Sep;2(9):669-77. doi: 10.1093/molehr/2.9.669. Mol Hum Reprod. 1996. PMID: 9239681 Review.

2

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

3

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

4

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

5

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

6

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

7

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: ferec c. Hum Mol Genet. 1993 Jan;2(1):51-4. doi: 10.1093/hmg/2.1.51. Hum Mol Genet. 1993. PMID: 7683952

8

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: ferec c. Hum Genet. 1996 Aug;98(2):223-7. doi: 10.1007/s004390050196. Hum Genet. 1996. PMID: 8698348

9

Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers.

Morral N, Dörk T, Llevadot R, Dziadek V, Mercier B, Férec C, Costes B, Girodon E, Zielenski J, Tsui LC, Tümmler B, Estivill X. Morral N, et al. Among authors: ferec c. Hum Mutat. 1996;8(2):149-59. doi: 10.1002/(SICI)1098-1004(1996)8:2<149::AID-HUMU7>3.0.CO;2-6. Hum Mutat. 1996. PMID: 8844213

10

Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities.

Lissens W, Mercier B, Tournaye H, Bonduelle M, Férec C, Seneca S, Devroey P, Silber S, Van Steirteghem A, Liebaers I. Lissens W, et al. Among authors: ferec c. Hum Reprod. 1996 Dec;11 Suppl 4:55-78; discussion 79-80. doi: 10.1093/humrep/11.suppl_4.55. Hum Reprod. 1996. PMID: 9147111 Review.

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