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Results: 1-5 |
Results: 5

Authors: Colleaux, L Rio, M Heuertz, S Moindrault, S Turleau, C Ozilou, C Gosset, P Raoult, O Lyonnet, S Cormier-Daire, V Amiel, J Le Merrer, M Picq, M de Blois, MC Prieur, M Romana, S Cornelis, F Vekemans, M Munnich, A
Citation: L. Colleaux et al., A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation, EUR J HUM G, 9(5), 2001, pp. 319-327

Authors: Holder-Espinasse, M de Blois, MC Faivre, L Romana, S Uteza, Y Munnich, A Lyonnet, S Cormier-Daire, V Amiel, J
Citation: M. Holder-espinasse et al., Absent lacrimal ducts, distichiasis, dysmorphic features, and brachydactyly: a case report, CLIN DYSMOR, 10(4), 2001, pp. 253-255

Authors: De Leersnyder, H de Blois, MC Claustrat, B Romana, S Albrecht, U von Kleist-Retzow, JC Delobel, B Viot, G Lyonnet, S Vekemans, M Munnich, A
Citation: H. De Leersnyder et al., Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome, J PEDIAT, 139(1), 2001, pp. 111-116

Authors: De Leersnyder, H de Blois, MC Vekemans, M Sidi, D Villain, E Kindermans, C Munnich, A
Citation: H. De Leersnyder et al., beta(1)-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome, J MED GENET, 38(9), 2001, pp. 586-590

Authors: Joly, G Lapierre, JM Ozilou, C Gosset, P Aurias, A de Blois, MC Prieur, M Raoul, O Colleaux, L Munnich, A Romana, SP Vekemans, M Turleau, C
Citation: G. Joly et al., Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype, CLIN GENET, 60(3), 2001, pp. 212-219
Risultati: 1-5 |