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Prenatal diagnosis of cystic fibrosis by multiplex PRC of mutation and microsatellite allelesESTIVILL, X; MORRAL, N; CASALS, T et al.Lancet (British edition). 1991, Vol 338, Num 8764, issn 0140-6736, p. 458Article

Pregnancy in patients with cystic fibrosisPALMER, J; DILLON-BAKER, C; TECKLIN, J. S et al.Annals of internal medicine. 1983, Vol 99, Num 5, pp 596-600, issn 0003-4819Article

Cystic fibrosisDAVIS, P. B.Seminars in respiratory medicine. 1985, Vol 6, Num 4, pp 243-340, issn 0192-9755Serial Issue

Towards the biochemical defect in cystic fibrosisLancet (British edition). 1989, Vol 2, Num 8677, issn 0140-6736, 1433 [1 p.]Article

Quantification of chloride in sweat with the cystic fibrosis indicator system^®WARWICK, W. J; HANSEN, L. G; WERNESS, M. E et al.Clinical chemistry (Baltimore, Md.). 1990, Vol 36, Num 1, pp 96-98, issn 0009-9147, 3 p.Article

Cystic fibrosis and seizuresO'MAHONY, M. S; FITZGERALD, M. X.Lancet (British edition). 1991, Vol 338, Num 8761, issn 0140-6736, p. 259Article

Nutrient intake of patients with cystic fibrosisHODGES, P; SAURIOL, D; MAN, S. F. P et al.Journal of the American Dietetic Association. 1984, Vol 84, Num 6, pp 664-669, issn 0002-8223Article

Cystic fibrosis serum does not inhibit human ciliary beat frequencyRUTLAND, J; PENKETH, A; GRIFFIN, W. M et al.The American review of respiratory disease. 1983, Vol 128, Num 6, pp 1030-1034, issn 0003-0805Article

Screening for cystic fibrosisSTEWART, A. D.Nature (London). 1989, Vol 342, Num 6244, issn 0028-0836, 696Article

Dépistage de la mucoviscidose : conséquences attenduesSARLES, J.LES DOSSIERS DE L'OBSTETRIQUE. 1998, Num 263, pp 35-36Article

The cystic fibrosis geneSCAMBLER, P. J.Archives of disease in childhood. 1989, Vol 64, Num 12, pp 1647-1648, issn 0003-9888Article

La mucoviscidose en France en 1988 = Cystic fibrosis in France in 1988LENOIR, G; SIMON, G; BARBIER, O et al.Annales de pédiatrie (Paris). 1988, Vol 35, Num 9, pp 623-625, issn 0066-2097Article

Is salt reabsorption in the human sweat duct subject to control?SCHWARZ, V; NAOMI SIMPSON, I. M.Clinical science (1979). 1985, Vol 68, Num 4, pp 441-447, issn 0143-5221Article

Massive hemoptysis in cystic fibrosisPORTER, D. K; VAN EVERY, M. J; ANTHRACITE, R. F et al.Archives of internal medicine (1960). 1983, Vol 143, Num 2, pp 287-290, issn 0003-9926Article

Carcinoembryonic antigen, α₁-antitrypsin, and α-fetoprotein in the pancreas of patients with cystic fibrosisSCHEELE, P. M; BENDON, R. W; RAY, M. B et al.Archives of pathology & laboratory medicine (1976). 1989, Vol 113, Num 10, pp 1142-1146, issn 0363-0153, 5 p.Article

Effectiveness of prevention of cystic fibrosis by artificial insemination by donor can be markedly improved by DNA-analysis of sperm donorsTEN KATE, L. P; TE MEERMAN, G. J; BUYS, C. H. C. M et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 148-149, issn 0148-7299, 2 p.Article

Hypertrophic osteoarthropathy in cystic fibrosisBRAUDE, S; KENNEDY, H; HODSON, M et al.British medical journal (1857). 1984, Vol 288, Num 6420, pp 822-823, issn 0007-1447Article

Conseils d'alimentation à un enfant atteint de mucoviscidose = Dietetic advice to the child with mucoviscidosisLENOIR, G; ASTRE, J; DUHAMEL, J. F et al.Concours médical (Paris). 1984, Vol 106, Num 23, pp 2173-2178, issn 0010-5309Article

Methylprednisolone resistance of cystic fibrosis lymphocytesLANGHOFF, E; PEDERSEN, P. S; KOCH, C et al.Pediatric research. 1984, Vol 18, Num 5, pp 488-489, issn 0031-3998Article

La mucoviscidose: manifestations digestives chez l'enfant et formes mono-symptomatiques = Mucoviscidosis: digestive symptomatology in the child and monosymptomatic formsBUTS, J.-P.Acta gastro-enterologica belgica (Ed. multilingue). 1984, Vol 47, Num 2, pp 132-133, issn 0001-5644Article

Mucoviscidose chez un enfant africain: à propos d'un cas = Mucoviscidosis in an african child. A case reportDEMAY, G; CHERON, G; CHALLIER, P et al.Archives françaises de pédiatrie. 1984, Vol 41, Num 5, issn 0003-9764, 370Article

Covalently linked fatty acids in gastric mucus glycoprotein of cystic fibrosis patientsSLOMIANY, A; WITAS, H; AONO, M et al.The Journal of biological chemistry (Print). 1983, Vol 258, Num 14, pp 8535-8538, issn 0021-9258Article

Development of a screening system for cystic fibrosisCOURY, A. J; FOGT, E. J; SUE NORENBERG, M et al.Clinical chemistry (Baltimore, Md.). 1983, Vol 29, Num 9, pp 1593-1597, issn 0009-9147Article

Cystic fibrosis gene mutations, and correlation with clinical manifestationPIGNATTI, P. F.Pathologie et biologie. 1991, Vol 39, Num 6, pp 582-584, issn 0369-8114Conference Paper