J. Riordan, J. Rommens, B. Kerem, N. Alon, R. Rozmahel et al., Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA, Science, vol.245, issue.4922, pp.1066-73, 1989.
DOI : 10.1126/science.2475911

M. Welsh, B. Ramsey, F. Accurso, G. Cutting, C. Scriver et al., Cystic fibrosis. In The Metabolic and Molecular Basis of Inherited Disease, pp.5121-88

K. Southern, A. Munck, R. Pollitt, G. Travert, L. Zanolla et al., A survey of newborn screening for cystic fibrosis in Europe, Journal of Cystic Fibrosis, vol.6, issue.1, pp.57-65, 2007.
DOI : 10.1016/j.jcf.2006.05.008

D. Salvatore, R. Buzzetti, E. Baldo, M. Forneris, V. Lucidi et al., An overview of international literature from cystic fibrosis registries. Part 3. Disease incidence, genotype/phenotype correlation, microbiology, pregnancy, clinical complications, lung transplantation, and miscellanea, Journal of Cystic Fibrosis, vol.10, issue.2, pp.71-85, 2011.
DOI : 10.1016/j.jcf.2010.12.005

J. Dodge, S. Morison, P. Lewis, E. Coles, D. Geddes et al., Incidence, population, and survival of cystic fibrosis in the UK, Arch Dis Child, vol.77, pp.1968-95493, 1997.

A. Dupuis, D. Hamilton, D. Cole, and M. Corey, Cystic Fibrosis Birth Rates in Canada: A Decreasing Trend since the Onset of Genetic Testing, The Journal of Pediatrics, vol.147, issue.3, pp.312-317, 2005.
DOI : 10.1016/j.jpeds.2005.06.043

M. Slieker, C. Uiterwaal, M. Sinaasappel, H. Heijerman, L. Van-der et al., Birth Prevalence and Survival in Cystic Fibrosis, Chest, vol.128, issue.4, pp.2309-2324, 2005.
DOI : 10.1378/chest.128.4.2309

M. Green, L. Weaver, A. Heeley, K. Nicholson, J. Kuzemko et al., Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural history., Archives of Disease in Childhood, vol.68, issue.4, pp.464-471, 1993.
DOI : 10.1136/adc.68.4.464

M. Super, M. Schwarz, G. Malone, T. Roberts, A. Haworth et al., Active cascade testing for carriers of cystic fibrosis gene, BMJ, vol.308, issue.6942, pp.1462-1469, 1994.
DOI : 10.1136/bmj.308.6942.1462

M. Mennie, A. Gilfillan, M. Compton, L. Curtis, W. Liston et al., Prenatal screening for cystic fibrosis, The Lancet, vol.340, issue.8813, pp.214-220, 1992.
DOI : 10.1016/0140-6736(92)90476-J

J. Hale, R. Parad, and A. Comeau, Newborn Screening Showing Decreasing Incidence of Cystic Fibrosis, New England Journal of Medicine, vol.358, issue.9, pp.973-977, 2008.
DOI : 10.1056/NEJMc0707530

C. Castellani, L. Picci, A. Tamanini, P. Girardi, P. Rizzotti et al., Association Between Carrier Screening and Incidence of Cystic Fibrosis, JAMA, vol.302, issue.23, pp.2573-2582, 2009.
DOI : 10.1001/jama.2009.1758

V. Scotet, D. Gillet, I. Duguépéroux, M. Audrézet, G. Bellis et al., Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960, Human Genetics, vol.111, issue.3, pp.247-54, 2002.
DOI : 10.1007/s00439-002-0788-1

V. Scotet, D. Braekeleer, M. Roussey, M. Rault, G. Parent et al., Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis, The Lancet, vol.356, issue.9232, pp.789-94, 2000.
DOI : 10.1016/S0140-6736(00)02652-0

S. Mayell, A. Munck, J. Craig, I. Sermet, K. Brownlee et al., A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis, Journal of Cystic Fibrosis, vol.8, issue.1, pp.71-79, 2009.
DOI : 10.1016/j.jcf.2008.09.005

E. Dequeker, M. Stuhrmann, M. Morris, T. Casals, C. Castellani et al., Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders ??? updated European recommendations, European Journal of Human Genetics, vol.6, issue.1, pp.51-65, 2009.
DOI : 10.1136/jmg.2003.015065

C. Castellani, H. Cuppens, M. Macek, . Jr, J. Cassiman et al., Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice, Journal of Cystic Fibrosis, vol.7, issue.3, pp.179-96, 2008.
DOI : 10.1016/j.jcf.2008.03.009

A. Dobson and A. Barnett, An introduction to generalized linear models. 3 edition. Chapman and Hall/CRC, 2008.

D. Brock, Amniotic fluid alkaline phosphatase isoenzymes in early prenatal diagnosis of cystic fibrosis, Lancet, vol.2, pp.941-944, 1983.

I. Mcintosh, J. Raeburn, A. Curtis, and D. Brock, FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY DIRECT GENE PROBING, The Lancet, vol.334, issue.8669, pp.972-975, 1989.
DOI : 10.1016/S0140-6736(89)90974-4

V. Scotet, I. Duguépéroux, M. Audrézet, M. Blayau, P. Boisseau et al., Prenatal diagnosis of cystic fibrosis: the 18-year experience of Brittany (western France), Prenatal Diagnosis, vol.12, issue.3, pp.197-202, 2008.
DOI : 10.1002/pd.1910

B. Rosenstein and G. Cutting, WHAT IS A CYSTIC FIBROSIS DIAGNOSIS?, Clinics in Chest Medicine, vol.19, issue.3, pp.589-95, 1998.
DOI : 10.1016/S0272-5231(05)70091-5

P. Farrell, B. Rosenstein, T. White, F. Accurso, C. Castellani et al., Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report, The Journal of Pediatrics, vol.153, issue.2, pp.4-14, 2008.
DOI : 10.1016/j.jpeds.2008.05.005

M. Sontag, J. Wagener, F. Accurso, and S. Sagel, Consistent incidence of cystic fibrosis in a long-term newborn screen population [abstract]. Pediat Pulmonol, A203), p.272, 2008.

T. Kate and L. , Cystic fibrosis in the Netherlands, International Journal of Epidemiology, vol.6, issue.1, pp.23-34, 1977.
DOI : 10.1093/ije/6.1.23

J. Massie, L. Curnow, L. Gaffney, J. Carlin, and I. Francis, Declining prevalence of cystic fibrosis since the introduction of newborn screening, Archives of Disease in Childhood, vol.95, issue.7, pp.531-534, 2010.
DOI : 10.1136/adc.2009.172916

D. Stachiw-hietpas, G. Hoffman, M. Nugent, K. Schneck, K. Kennedy-parker et al., Wisconsin newborn screening program results suggest a decreasing incidence of CF in the white nonhispanic population, A474), p.390, 2010.

A. Cao, M. Rosatelli, G. Monni, and R. Galanello, Screening for thalassemia, Obstetrics and Gynecology Clinics of North America, vol.29, issue.2, pp.305-333, 2002.
DOI : 10.1016/S0889-8545(01)00006-7