Showing 1 - 4 results of 4 for search 'Saugier-Veber, P', query time: 0.02s
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Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome? by Saugier-Veber, P, Munnich, A, Lyonnet, S, Toutain, A, Moraine, C, Piussan, C, Mathieu, M, Gibbons, R
Published 1995Journal article -
2
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. by Koolen, D, Sharp, A, Hurst, J, Firth, H, Knight, S, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L, Destrée, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M, Mancini, G, Poddighe, P, Schwartz, C, Rossi, E, De Gregori, M, Antonacci-Fulton, L, McLellan, MD, Garrett, J
Published 2008Journal article -
3
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome by Koolen, D, Sharp, A, Hurst, J, Firth, H, Knight, S, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L, Destree, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M, Mancini, G, Poddighe, P, Schwartz, C, Rossi, E, De Gregori, M, Antonacci-Fulton, L, Ii, M, Garrett, J
Published 2008Journal article -
4
Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosis by Chatron, N, Cassinari, K, Quenez, O, Baert-Desurmont, S, Bardel, C, Buisine, M, Calpena, E, Capri, Y, Galbany, J, Diguet, F, Edery, P, Isidor, B, Labalme, A, Le Caignec, C, Lévy, J, Lecoquierre, F, Lindenbaum, P, Pichon, O, Rollat-Farnier, P, Simonet, T, Saugier-Veber, P, Tabet, A, Toutain, A, Wilkie, A, Lesca, G, Sanlaville, D, Nicolas, G, Schluth-Bolard, C
Published 2019Journal article