Chaventré A - Search Results

1

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: chaventre a. Lancet. 2000 Sep 2;356(9232):789-94. doi: 10.1016/S0140-6736(00)02652-0. Lancet. 2000. PMID: 11022925

2

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

3

[Gene mutations of cystic fibrosis in Brittany population].

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

4

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

5

Genetic factors in iodine deficiency disorders: a general review.

De Braekeleer M, Mayer G, Chaventré A. De Braekeleer M, et al. Among authors: chaventre a. Coll Antropol. 1998 Jun;22(1):9-15. Coll Antropol. 1998. PMID: 10097415 Review.

6

[Linkage between juvenile glaucoma and chromosome 1q in 2 French families].

Meyer A, Valtot F, Béchetoille A, Rouland JF, Dascotte JC, Férec C, Bach JF, Chaventré A, Garchon HJ. Meyer A, et al. Among authors: chaventre a. C R Acad Sci III. 1994 Jun;317(6):565-70. C R Acad Sci III. 1994. PMID: 7987708 French.

7

[Assessment of risk factors in the case of endemic goiter in Ivory Coast].

Bellis G, Chaventré A, Kouamé P, Roux F, Gaimard M, Dilumbu I, Assouan A, De Braekeleer M. Bellis G, et al. Among authors: chaventre a. Rev Epidemiol Sante Publique. 2000 Apr;48(2):212-3. Rev Epidemiol Sante Publique. 2000. PMID: 10804429 French. No abstract available.

8

An mtDNA perspective of French genetic variation.

Richard C, Pennarun E, Kivisild T, Tambets K, Tolk HV, Metspalu E, Reidla M, Chevalier S, Giraudet S, Lauc LB, Pericić M, Rudan P, Claustres M, Journel H, Dorval I, Müller C, Villems R, Chaventré A, Moisan JP. Richard C, et al. Among authors: chaventre a. Ann Hum Biol. 2007 Jan-Feb;34(1):68-79. doi: 10.1080/03014460601076098. Ann Hum Biol. 2007. PMID: 17536756

9

Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.

Le Caignec C, Lefevre M, Schott JJ, Chaventre A, Gayet M, Calais C, Moisan JP. Le Caignec C, et al. Among authors: chaventre a. Am J Hum Genet. 2002 Jul;71(1):180-6. doi: 10.1086/341327. Epub 2002 May 17. Am J Hum Genet. 2002. PMID: 12022040 Free PMC article.

10

DNA short tandem repeat profiling of Morocco.

Jauffrit A, El Amri H, Airaud F, André MT, Herbert O, Landeau-Trottier G, Giraudet S, Richard C, Chaventré A, Moisan JP. Jauffrit A, et al. Among authors: chaventre a. J Forensic Sci. 2003 Mar;48(2):458-9. J Forensic Sci. 2003. PMID: 12665020 No abstract available.

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