Férec C - Search Results

1

ABL1 fusion genes in hematological malignancies: a review.

De Braekeleer E, Douet-Guilbert N, Rowe D, Bown N, Morel F, Berthou C, Férec C, De Braekeleer M. De Braekeleer E, et al. Among authors: ferec c. Eur J Haematol. 2011 May;86(5):361-71. doi: 10.1111/j.1600-0609.2011.01586.x. Epub 2011 Mar 23. Eur J Haematol. 2011. PMID: 21435002 Review.

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. 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.

3

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada).

Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M. Rivard SR, et al. Among authors: ferec c. Br J Haematol. 2000 Mar;108(4):854-8. doi: 10.1046/j.1365-2141.2000.01954.x. Br J Haematol. 2000. PMID: 10792295 Free article.

4

Nramp2 analysis in hemochromatosis probands.

Le Gac G, Mura C, Raguenes O, Mercier AY, de Braekeleer M, Férec C. Le Gac G, et al. Among authors: ferec c. Blood Cells Mol Dis. 2000 Aug;26(4):312-9. doi: 10.1006/bcmd.2000.0312. Blood Cells Mol Dis. 2000. PMID: 11042033

5

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: ferec c. Coll Antropol. 2000 Dec;24(2):281-6. Coll Antropol. 2000. PMID: 11216394

6

Relationship between genotype and phenotype for the CFTR gene W846X mutation.

Duguépéroux I, Bellis G, Férec C, Gillet D, Scotet V, De Braekeleer M; Participating centres of the French CF registry. Duguépéroux I, et al. Among authors: ferec c. J Med Genet. 2002 Jun;39(6):E32. doi: 10.1136/jmg.39.6.e32. J Med Genet. 2002. PMID: 12070264 Free PMC article. No abstract available.

7

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: ferec c. Hum Genet. 2003 Aug;113(3):280-5. doi: 10.1007/s00439-003-0962-0. Epub 2003 May 27. Hum Genet. 2003. PMID: 12768409

8

Prenatal diagnosis of mosaic tetrasomy 8p.

Le Bris MJ, Marcorelles P, Audrézet MP, Parent P, Heren P, Le Guern H, Herry A, Morel F, Collet M, Férec C, De Braekeleer M. Le Bris MJ, et al. Among authors: ferec c. Am J Med Genet A. 2003 Jul 1;120A(1):44-8. doi: 10.1002/ajmg.a.20199. Am J Med Genet A. 2003. PMID: 12794691

9

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: ferec c. Hum Mutat. 2003 Jul;22(1):105. doi: 10.1002/humu.9158. Hum Mutat. 2003. PMID: 12815607

10

Diagnosis and outcome of complete hydatidiform mole coexisting with a live twin fetus.

Marcorelles P, Audrezet MP, Le Bris MJ, Laurent Y, Chabaud JJ, Ferec C, de Braekeleer M, Collet M, Lagarde N. Marcorelles P, et al. Among authors: ferec c. Eur J Obstet Gynecol Reprod Biol. 2005 Jan 10;118(1):21-7. doi: 10.1016/j.ejogrb.2004.02.042. Eur J Obstet Gynecol Reprod Biol. 2005. PMID: 15596267

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

568 results

Search Page