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Archives Francaises De Pediatrie|October 1, 1987
[Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy]F Rey, M Berthelon, A Munnich, et al.American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.Human Genetics|January 1, 1985
Maple syrup urine disease: two different forms within a single familyJ Frézal, O Amédée-Manesme, G Mitchell, et al.Journal of Inherited Metabolic Disease|January 1, 1984
Hudson memorial lecture. Neonatal management of organic acidurias. Clinical updateJ M Saudubray, H Ogier, C Charpentier, et al.Archives Francaises De Pediatrie|November 1, 1992
[Intellectual development after relaxing the diet at the age of 5 years in typical phenylketonuria]V Abadie, F Rey, F Plainguet, et al.European Journal of Pediatrics|July 1, 1996
Long-term follow up of patients with classical phenylketonuria after diet relaxation at 5 years of age. The Paris StudyF Rey, V Abadie, F Plainguet, et al.Pediatric Research|March 1, 1997
Neuropsychologic functions of early treated patients with phenylketonuria, on and off diet: results of a cross-national and cross-sectional studyP Burgard, F Rey, A Rupp, et al.Archives of Disease in Childhood|August 1, 1980
Biopterin defect in a normal-appearing child affected by a transient phenylketonuriaF Rey, R J Leeming, J A Blair, et al.Bulletin De L'Academie Nationale De Medecine|December 1, 1995
[Fifty years of medical genetics. A tribute to Maurice Lamy on the hundredth anniversary of his birth]J FrézalComptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 3, 1998
Genatlas database, genes and development defectsJ FrézalPageof 64