1. Neonatal screening;Dankert-Roelse, J.E.,1994
2. Abnormal frequency of AF508 mutation in neonatal transitory hypertrypsinaemia;Laroche, D.; Travert, G.;Lanicet,1991
3. Transient neonatal hypertrypsinaemia as test for AF508 heterozygosity;Lucotte, G.; Perignon, J.L.; Lenoir, G.;Lanlcet,1991
4. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens;Chillon, M.; Casals, T.; Mercier, B.;N Enigl I Med,1995
5. The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis;Oates, R.D.; Amos, J.A.;7 Anidrol,1994