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[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.
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
Prenatal diagnosis of Fryns' syndrome.
Pellissier MC, Philip N, Potier A, Scheiner C, Aymé S, Mattei JF, Giraud F. Pellissier MC, et al. Among authors: giraud f. Prenat Diagn. 1992 Apr;12(4):299-303. doi: 10.1002/pd.1970120410. Prenat Diagn. 1992. PMID: 1614987 Review.
[News in chromosome pathology].
Giraud F, Mattei JF. Giraud F, et al. Pediatrie. 1979 Dec;34(8):847-9. Pediatrie. 1979. PMID: 545283 French. No abstract available.
[The chromosome 13 in ring syndrome].
Giraud F, Emberger JM, Pinsard N, Mattei JF, Mattei MG. Giraud F, et al. Pediatrie. 1975 Jun;30(4):339-49. Pediatrie. 1975. PMID: 1178264 French. No abstract available.
Cerebrofaciothoracic dysplasia: a new family.
Philip N, Guala A, Moncla A, Monlouis M, Aymé S, Giraud F. Philip N, et al. Among authors: giraud f. J Med Genet. 1992 Jul;29(7):497-9. J Med Genet. 1992. PMID: 1640432 Free PMC article.
380 results