De Braekeleer M - Search Results

1

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

2

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. Mol Hum Reprod. 1996 Sep;2(9):669-77. doi: 10.1093/molehr/2.9.669. Mol Hum Reprod. 1996. PMID: 9239681 Review.

3

Complete identification of cystic fibrosis transmembrane conductance regulator mutations in the CF population of Saguenay Lac-Saint-Jean (Quebec, Canada).

De Braekeleer M, Mari C, Verlingue C, Allard C, Leblanc JP, Simard F, Aubin G, Férec C. De Braekeleer M, et al. Clin Genet. 1998 Jan;53(1):44-6. doi: 10.1034/j.1399-0004.1998.531530108.x. Clin Genet. 1998. PMID: 9550360

4

Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960.

Scotet V, Gillet D, Duguépéroux I, Audrézet MP, Bellis G, Garnier B, Roussey M, Rault G, Parent P, De Braekeleer M, Férec C; Réseau Mucoviscidose Bretagne et Pays de Loire. Scotet V, et al. Among authors: de braekeleer m. Hum Genet. 2002 Sep;111(3):247-54. doi: 10.1007/s00439-002-0788-1. Epub 2002 Aug 1. Hum Genet. 2002. PMID: 12215837

5

Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France.

Scotet V, Audrézet MP, Roussey M, Rault G, Blayau M, De Braekeleer M, Férec C. Scotet V, et al. Among authors: de braekeleer m. Hum Genet. 2003 Aug;113(3):280-5. doi: 10.1007/s00439-003-0962-0. Epub 2003 May 27. Hum Genet. 2003. PMID: 12768409

6

Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation.

De Braekeleer M, Allard C, Leblanc JP, Simard F, Aubin G. De Braekeleer M, et al. Hum Genet. 1997 Dec;101(2):208-11. doi: 10.1007/s004390050616. Hum Genet. 1997. PMID: 9402971

7

Clinical features of cystic fibrosis patients with rare genotypes in Saguenay Lac-Saint-Jean (Quebec, Canada).

de Braekeleer M, Mari G, Verlingue C, Allard C, Leblanc JP, Simard F, Aubin G, Férec C. de Braekeleer M, et al. Ann Genet. 1997;40(4):205-8. Ann Genet. 1997. PMID: 9526613

8

Correlation between mutations and age in cystic fibrosis in a French Canadian population.

Rivard SR, Allard C, Leblanc JP, Milot M, Aubin G, Simard F, Férec C, de Braekeleer M. Rivard SR, et al. Among authors: de braekeleer m. J Med Genet. 2000 Mar;37(3):225-7. doi: 10.1136/jmg.37.3.225. J Med Genet. 2000. PMID: 10777368 Free PMC article. No abstract available.

9

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

10

Microsatellite haplotypes associations with 5 CFTR mutations in "Grande Brière", an isolate located in southern Brittany.

Bezieau S, Picherot G, David A, De Braekeleer M, Ferec C, Moisan JP, Chaventré A. Bezieau S, et al. Among authors: de braekeleer m. Coll Antropol. 2000 Dec;24(2):281-6. Coll Antropol. 2000. PMID: 11216394

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