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Results: 1-4 |
Results: 4

Authors: Zannolli, R Mostardini, R Carpentieri, ML Gatti, MG Galluzzi, P Vagnoli, PT Giorgetti, R Calvieri, S Morgese, G
Citation: R. Zannolli et al., Cranioectodermal dysplasia: A new patient with an inapparent, subtle phenotype, PEDIAT DERM, 18(4), 2001, pp. 332-335

Authors: Zannolli, R Mostardini, R Pucci, L Sorrentino, L Biagioli, M Perotti, R Guarna, M Hadjistilianou, T Zerega, G Pierluigi, M Franco, B D'Ambrosio, A Morgese, G
Citation: R. Zannolli et al., Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;14) (pter;q11.2)], AM J MED G, 102(1), 2001, pp. 29-35

Authors: Zannolli, R Mostardini, R Hadjistilianou, T Rosi, A Berardi, R Morgese, G
Citation: R. Zannolli et al., MOMO syndrome: a possible third case, CLIN DYSMOR, 9(4), 2000, pp. 281-284

Authors: Zannolli, R Mostardini, R Matera, M Pucci, L Gelb, BD Morgese, G
Citation: R. Zannolli et al., Char syndrome: An additional family with polythelia, a new finding, AM J MED G, 95(3), 2000, pp. 201-203
Risultati: 1-4 |