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Genomics|November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuriaV Abadie, S Lyonnet, N Maurin, et al.The Journal of Biological Chemistry|May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuriaC Caillaud, S Lyonnet, F Rey, et al.Journal of Medical Genetics|August 1, 1995
Filippi syndrome: a new case with skeletal abnormalitiesD Héron, T Billette de Villemeur, A Munnich, et al.Presse Medicale (Paris, France : 1983)|November 2, 1996
[Advances in genetics: what benefits children?]S Lyonnet, J P Bonnefont, M L Briard, et al.The Journal of Clinical Investigation|June 1, 1988
In vivo regulation of glycolytic and gluconeogenic enzyme gene expression in newborn rat liverS Lyonnet, C Coupé, J Girard, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|June 1, 1975
[Prevention of congenital toxoplasmosis. Results at the maternity department of the Hôpital Saint-Antoine in 1972]C Roux, G Desmonts, M Gaulier, et al.American Journal of Human Genetics|December 1, 1988
Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in FranceF Rey, M Berthelon, C Caillaud, et al.Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Identification of mutation of RET proto-oncogene in Hirschsprung disease]T Attié, P Edery, S Lyonnet, et al.The Journal of Biological Chemistry|December 15, 1987
Differential effects of glucose and fructose on liver L-type pyruvate kinase gene expression in vivoA Munnich, S Lyonnet, D Chauvet, et al.Medical Hypotheses|June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesisL Faivre, J P Bonnefont, S Lyonnet, et al.Pageof 117