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• Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG).

  [No authors listed] [No authors listed] Hum Genet. 1990 Sep;85(4):436-45. doi: 10.1007/BF02428304. Hum Genet. 1990. PMID: 2210767 Clinical Trial.
• Linkage disequilibrium of three polymorphic RFLP markers in the apolipoprotein AI-CIII gene cluster on chromosome 11.

  Marasco O, Melina F, Mele E, Quaresima B, Zingone A, Focarelli E, Picciotti E, Martelli ML, Fotino L, Vigna MF, et al. Marasco O, et al. Hum Genet. 1993 Mar;91(2):169-74. doi: 10.1007/BF00222719. Hum Genet. 1993. PMID: 8096493
• Why is the cystic fibrosis gene so frequent?

  Romeo G, Devoto M, Galietta LJ. Romeo G, et al. Hum Genet. 1989 Dec;84(1):1-5. doi: 10.1007/BF00210660. Hum Genet. 1989. PMID: 2691388 Review.
• Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France.

  Rey F, Berthelon M, Caillaud C, Lyonnet S, Abadie V, Blandin-Savoja F, Feingold J, Saudubray JM, Frézal J, Munnich A, et al. Rey F, et al. Am J Hum Genet. 1988 Dec;43(6):914-21. Am J Hum Genet. 1988. PMID: 2904221 Free PMC article.
• Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population.

  Vidaud M, Kitzis A, Ferec C, Bozon D, Dumur V, Giraud G, David F, Pascal O, Auvinet M, Morel Y, et al. Vidaud M, et al. Hum Genet. 1989 Jan;81(2):183-4. doi: 10.1007/BF00293899. Hum Genet. 1989. PMID: 2563252