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Page 1
Association of 1078 del T cystic fibrosis mutation with severe disease.
Moullier P, Jéhanne M, Audrézet MP, Mercier B, Verlingue C, Quéré I, Guillermit H, Raguénès O, Storni V, Rault G, et al. Moullier P, et al. Among authors: rault g. J Med Genet. 1994 Feb;31(2):159-61. doi: 10.1136/jmg.31.2.159. J Med Genet. 1994. PMID: 7514227 Free PMC article.
Identification of 12 novel mutations in the CFTR gene.
Audrézet MP, Mercier B, Guillermit H, Quéré I, Verlingue C, Rault G, Férec C. Audrézet MP, et al. Among authors: rault g. Hum Mol Genet. 1993 Jan;2(1):51-4. doi: 10.1093/hmg/2.1.51. Hum Mol Genet. 1993. PMID: 7683952
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: rault g. Lancet. 2000 Sep 2;356(9232):789-94. doi: 10.1016/S0140-6736(00)02652-0. Lancet. 2000. PMID: 11022925
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: rault g. Hum Genet. 2002 Sep;111(3):247-54. doi: 10.1007/s00439-002-0788-1. Epub 2002 Aug 1. Hum Genet. 2002. PMID: 12215837
80 results