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Exclusion of anionic trypsinogen and mesotrypsinogen involvement in hereditary pancreatitis without cationic trypsinogen gene mutations.
Chen JM, Audrezet MP, Mercier B, Quere I, Ferec C. Chen JM, et al. Scand J Gastroenterol. 1999 Aug;34(8):831-2. doi: 10.1080/003655299750025796. Scand J Gastroenterol. 1999. PMID: 10499487 No abstract available.
Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
Férec C, Raguénès O, Salomon R, Roche C, Bernard JP, Guillot M, Quéré I, Faure C, Mercier B, Audrézet MP, Guillausseau PJ, Dupont C, Munnich A, Bignon JD, Le Bodic L. Férec C, et al. J Med Genet. 1999 Mar;36(3):228-32. J Med Genet. 1999. PMID: 10204851 Free PMC article.
[The hemochromatosis gene (HFE). Molecular analysis--diagnostic applications].
Ferec C, Raguenes O, Mercier AY, Le Faou T, Chanu B, Le Poupon AM, Mercier B, Mura C. Ferec C, et al. Transfus Clin Biol. 1998 Aug;5(4):283-9. doi: 10.1016/s1246-7820(98)80407-2. Transfus Clin Biol. 1998. PMID: 9789968 French.
[Cystic fibrosis gene mutations in the West of France: clinical application].
Verlingue C, Travert G, Le Roux MG, Laroche D, Audrézet MP, Mercier B, Moisan JP, Férec C. Verlingue C, et al. Ann Biol Clin (Paris). 1994;52(11):757-64. Ann Biol Clin (Paris). 1994. PMID: 7747883 French.
Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresis.
Férec C, Verlingue C, Audrézet MP, Guillermit H, Quéré I, Raguenes O, Mercier B. Férec C, et al. Fetal Diagn Ther. 1993 Sep-Oct;8(5):341-50. doi: 10.1159/000263850. Fetal Diagn Ther. 1993. PMID: 7505587
Molecular analysis of the TP53 gene in Barrett's adenocarcinoma.
Audrézet MP, Robaszkiewicz M, Mercier B, Nousbaum JB, Hardy E, Bail JP, Volant A, Lozac'h P, Gouérou H, Férec C. Audrézet MP, et al. Hum Mutat. 1996;7(2):109-13. doi: 10.1002/(SICI)1098-1004(1996)7:2<109::AID-HUMU4>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8829627
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