AAAAAA

   
Results: 1-11 |
Results: 11

Authors: Tartaglia, M Mehler, EL Goldberg, R Zampino, G Brunner, HG Kremer, H van der Burgt, I Crosby, AH Ion, A Jeffery, S Kalidas, K Patton, MA Kucherlapati, RS Gelb, BD
Citation: M. Tartaglia et al., Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome, NAT GENET, 29(4), 2001, pp. 465-468

Authors: Tartaglia, M Mehler, EL Goldberg, R Zampino, G Brunner, HG Kremer, H van der Burgt, I Crosby, AH Ion, A Jeffery, S Kalidas, K Patton, MA Kucherlapati, RS Gelb, B
Citation: M. Tartaglia et al., Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan Syndrome (vol 29, pg 465, 2001), NAT GENET, 29(4), 2001, pp. 491-491

Authors: Tandoi, C Botta, A Fini, G Sangiuolo, F Novelli, G Ricci, R Zampino, G Anichini, C Dallapiccola, B
Citation: C. Tandoi et al., Exclusion of the elastin gene in the pathogenesis of Costello syndrome, AM J MED G, 98(3), 2001, pp. 286-287

Authors: Stoll, C Rosano, A Botto, LD Erickson, D Khoury, MJ Olney, RS Castilla, EE Cocchi, G Cornel, MC Goujard, J Bermejo, E Merlob, P Mutchinick, O Ritvanen, A Zampino, G Mastroiacovo, P
Citation: C. Stoll et al., On the symmetry of limb deficiencies among children with multiple congenital anomalies, ANN GENET, 44(1), 2001, pp. 19-24

Authors: Ruggiero, A Zampino, G Mastroiacovo, P Riccardi, R
Citation: A. Ruggiero et al., Diamond-blackfan anemia and midline defects, J PED H ONC, 22(5), 2000, pp. 479-480

Authors: De Pas, T de Braud, F Danesi, R Sessa, C Catania, C Curigliano, G Fogli, S del Tacca, M Zampino, G Sbanotto, A Rocca, A Cinieri, S Marrocco, E Milani, A Goldhirsch, A
Citation: T. De Pas et al., Phase I and pharmacologic study of weekly gemcitabine and paclitaxel in chemo-naive patients with advanced non-small-cell lung cancer, ANN ONCOL, 11(7), 2000, pp. 821-827

Authors: Zollino, M Di Stefano, C Zampino, G Mastroiacovo, P Wright, TJ Sorge, G Selicorni, A Tenconi, R Zappala, A Battaglia, A Di Rocco, M Palka, G Pallotta, R Altherr, MR Neri, G
Citation: M. Zollino et al., Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome, AM J MED G, 94(3), 2000, pp. 254-261

Authors: Rosano, A Botto, LD Olney, RS Khoury, MJ Ritvanen, A Goujard, J Stoll, C Cocchi, G Merlob, P Mutchinick, O Cornel, MC Castilla, EE Martinez-Frias, ML Zampino, G Erickson, JD Mastroiacovo, P
Citation: A. Rosano et al., Limb defects associated with major congenital anomalies: Clinical and epidemiological study from the international clearinghouse for birth defects monitoring systems, AM J MED G, 93(2), 2000, pp. 110-116

Authors: Zampino, G Balducci, F Mariotti, P Dickmann, A Mastroiacovo, P
Citation: G. Zampino et al., Growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia: Confirmation of the ROCA-Wiedemann syndrome, AM J MED G, 90(5), 2000, pp. 358-360

Authors: Arpino, C Brescianini, S Robert, E Castilla, EE Cocchi, G Cornel, MC de Vigan, C Lancaster, PAL Merlob, P Sumiyoshi, Y Zampino, G Renzi, C Resano, A Mastroiacovo, P
Citation: C. Arpino et al., Teratogenic effects of antiepileptic drugs: Use of an international database on malformations and drug exposure (MADRE), EPILEPSIA, 41(11), 2000, pp. 1436-1443

Authors: Pagani, O Sessa, C Martinelli, G Crivellari, D Buonadonna, A Thurlimann, B Hess, D Borner, M Bauer, J Zampino, G Zimatore, M Graffeo, R Riva, A Goldhirsch, A
Citation: O. Pagani et al., Dose-finding study of epidoxorubicin and docetaxel as first-line chemotherapy in patients with advanced breast cancer, ANN ONCOL, 10(5), 1999, pp. 539-545
Risultati: 1-11 |