Chaventre A - Search Results

1

[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.

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

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

4

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

5

[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.

6

Founder effect in GLC1A-linked familial open-angle glaucoma in Northern France.

Brézin AP, Adam MF, Belmouden A, Lureau MA, Chaventré A, Copin B, Gomez L, De Dinechin SD, Berkani M, Valtot F, Rouland JF, Dascotte JC, Bach JF, Garchon HJ. Brézin AP, et al. Among authors: chaventre a. Am J Med Genet. 1998 Apr 13;76(5):438-45. Am J Med Genet. 1998. PMID: 9556305

7

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.

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 Free article.

9

Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucoma.

Adam MF, Belmouden A, Binisti P, Brézin AP, Valtot F, Béchetoille A, Dascotte JC, Copin B, Gomez L, Chaventré A, Bach JF, Garchon HJ. Adam MF, et al. Among authors: chaventre a. Hum Mol Genet. 1997 Nov;6(12):2091-7. doi: 10.1093/hmg/6.12.2091. Hum Mol Genet. 1997. PMID: 9328473

10

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.

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