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Page 1
CpG dinucleotides are mutation hot spots in phenylketonuria.
Abadie V, Lyonnet S, Maurin N, Berthelon M, Caillaud C, Giraud F, Mattei JF, Rey J, Rey F, Munnich A. Abadie V, et al. Among authors: giraud f. Genomics. 1989 Nov;5(4):936-9. doi: 10.1016/0888-7543(89)90137-7. Genomics. 1989. PMID: 2574153
Achondroplasia in sibs of normal parents.
Philip N, Auger M, Mattei JF, Giraud F. Philip N, et al. Among authors: giraud f. J Med Genet. 1988 Dec;25(12):857-9. doi: 10.1136/jmg.25.12.857. J Med Genet. 1988. PMID: 3236371 Free PMC article.
[Linkage studies in Emery-Dreifuss muscular dystrophy].
Paquis V, Philip N, Voelckel MA, Pouget J, Lemieux B, Mattei JF, Giraud F. Paquis V, et al. Among authors: giraud f. J Genet Hum. 1989 Jun;37(2):127-32. J Genet Hum. 1989. PMID: 2746171 French.
The acrocallosal syndrome.
Philip N, Apicella N, Lassman I, Ayme S, Mattei JF, Giraud F. Philip N, et al. Among authors: giraud f. Eur J Pediatr. 1988 Feb;147(2):206-8. doi: 10.1007/BF00442226. Eur J Pediatr. 1988. PMID: 3366141
[Angelman syndrome].
Moncla A, Livet MO, Malzac P, Voelckel MA, Mattei MG, Mattei JF, Giraud F. Moncla A, et al. Among authors: giraud f. Arch Pediatr. 1994 Dec;1(12):1118-26. Arch Pediatr. 1994. PMID: 7849899 Review. French.
381 results