De Braekeleer M - Search Results

1

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

2

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

3

Comparison of the CFTR mutation spectrum in three cohorts of patients of Celtic origin from Brittany (France) and Ireland.

Scotet V, Barton DE, Watson JB, Audrézet MP, McDevitt T, McQuaid S, Shortt C, De Braekeleer M, Férec C, Le Maréchal C. Scotet V, et al. Among authors: de braekeleer m. Hum Mutat. 2003 Jul;22(1):105. doi: 10.1002/humu.9158. Hum Mutat. 2003. PMID: 12815607

4

Reproductive attitudes of couples having a child with cystic fibrosis in Brittany (France).

De Braekeleer M, Rault G, Bellis G. De Braekeleer M, et al. J Hum Genet. 2004;49(6):285-289. doi: 10.1007/s10038-004-0147-2. Epub 2004 Apr 23. J Hum Genet. 2004. PMID: 15105997

5

Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis.

Scotet V, de Braekeleer M, Roussey M, Rault G, Parent P, Dagorne M, Journel H, Lemoigne A, Codet JP, Catheline M, David V, Chaventré A, Duguépéroux I, Verlingue C, Quéré I, Mercier B, Audrézet MP, Férec C. Scotet V, et al. Among authors: de braekeleer m. Lancet. 2000 Sep 2;356(9232):789-94. doi: 10.1016/S0140-6736(00)02652-0. Lancet. 2000. PMID: 11022925

6

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

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

8

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.

9

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

10

[Neonatal screening for cystic fibrosis].

Scotet V, Audrézet MP, de Braekeleer M, Férec C. Scotet V, et al. Among authors: de braekeleer m. Pathol Biol (Paris). 2001 Dec;49(10):785-8. doi: 10.1016/s0369-8114(01)00245-0. Pathol Biol (Paris). 2001. PMID: 11776687 French. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

298 results

Search Page

Filters