Cougoureux E - Search Results

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Clinical evaluation of the CF(12)m cystic fibrosis DNA diagnostic kit.

Houdayer C, Cazeneuve C, Cougoureux E, Magnier C, Tredano M, Aymard P, Goossens M, Feldmann D. Houdayer C, et al. Among authors: cougoureux e. Clin Chem. 1998 Jun;44(6 Pt 1):1346-8. Clin Chem. 1998. PMID: 9625066 No abstract available.

CFTR gene analysis in cystic fibrosis patients: detection of 91% of molecular defects and identification of the novel mutation D979V.

Plouvier E, Cougoureux E, Sardet A, Tournier G, Aymard P, Feldmann D. Plouvier E, et al. Among authors: cougoureux e. Ann Genet. 1997;40(3):185-8. Ann Genet. 1997. PMID: 9401110 Clinical Trial.

Identification of three novel mutations in the CFTR gene, R117P, deltaD192, and 3121-1G-->A in four French patients.

Feldmann D, Sardet A, Cougoureux E, Plouvier E, Fontaine JL, Tournier G, Aymard P. Feldmann D, et al. Among authors: cougoureux e. Hum Mutat. 1998;Suppl 1:S78-80. doi: 10.1002/humu.1380110127. Hum Mutat. 1998. PMID: 9452048 No abstract available.

Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P).

Houdayer C, Bonaïti-Pellié C, Erguy C, Soupre V, Dondon MG, Bürglen L, Cougoureux E, Couderc R, Vazquez MP, Bahuau M. Houdayer C, et al. Among authors: cougoureux e. Am J Med Genet. 2001 Nov 15;104(1):86-92. doi: 10.1002/1096-8628(20011115)104:1<86::aid-ajmg10053>3.0.co;2-e. Am J Med Genet. 2001. PMID: 11746036

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