Showing 1 - 4 results of 4 for search 'Gimelli, G', query time: 0.02s
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Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome. by Jefferson, A, Colella, S, Moralli, D, Wilson, N, Yusuf, M, Gimelli, G, Ragoussis, I, Volpi, E
Published 2010Journal article -
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Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome by Jefferson, A, Colella, S, Moralli, D, Wilson, N, Yusuf, M, Gimelli, G, Ragoussis, J, Volpi, E
Published 2010Journal article -
3
Characterization of a recurrent 15q24 microdeletion syndrome. by Sharp, A, Selzer, R, Veltman, J, Gimelli, S, Gimelli, G, Striano, P, Coppola, A, Regan, R, Price, S, Knoers, N, Eis, P, Brunner, H, Hennekam, R, Knight, S, de Vries, B, Zuffardi, O, Eichler, E
Published 2007Journal article -
4
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. by Sharp, A, Mefford, H, Li, K, Baker, C, Skinner, C, Stevenson, R, Schroer, R, Novara, F, De Gregori, M, Ciccone, R, Broomer, A, Casuga, I, Wang, Y, Xiao, C, Barbacioru, C, Gimelli, G, Bernardina, B, Torniero, C, Giorda, R, Regan, R, Murday, V, Mansour, S, Fichera, M, Castiglia, L, Failla, P
Published 2008Journal article