Clinical management and molecular cytogenetic characterization in a 45,X/46,X,idic(Yp) patient with severe hypospadia von Marrocco, G, Poscente, M, Majore, S, De Bernardo, C, Rinaldi, R, Del Porto, G, Storniello, G, Grammatico, P

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Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families von Zachara, E, Caforio, A L, Carboni, G P, Pellegrini, A, Pompili, A, Del Porto, G, Sciarra, A, Bosman, C, Boldrini, R, Prati, P L

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Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis von VARESCO, L, GISMONDI, V, SALA, P, SASSATELLI, R, PONZ DE LEON, M, BIASCO, G, ALLEGRETTI, A, ASTE, H, DE SANCTIS, S, ROSSETTI, C, ILLENI, M. T, SCIARRA, A, JAMES, R, DEL PORTO, G, WHITE, R, GERRARA, G. B, ROBERTSON, M, GRAMMATICO, P, GRODEN, J, CASARINO, L, DE BENEDETTI, L, BAFICO, A, BERTARIO, L

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Increased Sensitivity to Peroxidative Agents as a Possible Pathogenic Factor of Melanocyte Damage in Vitiligo von Maresca, Vittoria, Roccella, Maria, Roccella, Francesca, Camera, Emanuela, Del Porto, Giuseppe, Passi, Siro, Grammatico, Paola, Picardo, Mauro

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Mutation in a splice-donor site of the APC gene in a family with polyposis and late age of colonic cancer death von VARESCO, L, GISMONDI, V, GRAMMATICO, P, DEL PORTO, G, WHITE, R, BERTARIO, L, FERRARA, G. B, PRESCIUTTINI, S, GRODEN, J, SPIRIO, L, SALA, P, ROSSETTI, C, DE BENEDETTI, L, BAFICO, A, HEOUAINE, A

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Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene : Clinical features and longitudinal observations von PANNARALE, M. R, GRAMMATICO, B, IANNACCONE, A, FORTE, R, DE BERNARDO, C, FLAGIELLO, L, VINGOLO, E. M, DEL PORTO, G

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The ocular phenotype of the Bardet-Biedl syndrome Comparison to non-syndromic retinitis pigmentosa von Iannaccone, Alessandro, Propris, Giampaolo De, Roncati, Stefania, Rispoli, Eduardo, Porto, Guiseppe Del, Pannarale, Mario R.

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Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online von Miano, M G, Valverde, D, Solans, T, Grammatico, B, Migliaccio, C, Cirigliano, V, DeBernardo, C, Ventruto, V, Meitinger, T, Wright, A, Del Porto, G, Baiget, M, D'Urso, M, Ciccodicola, A

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A low NM23.H1 gene expression identifying high malignancy human melanomas von Caligo, M A, Grammatico, P, Cipollini, G, Varesco, L, Del Porto, G, Bevilacqua, G

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Involvement of the 4q21 region in human malignant melanomas: Cytogenetic and immunocytochemical characterization of three primary cell cultures von Grammatico, P., Roccella, M., Catricalà, C., Roccella, F., Bucher, S., Mordenti, C., Amantea, A., Di Rosa, C., Del Porto, G.

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Cytogenetic and DNA Repair Studies in a Patient Affected by the Neonatal Progeroid Syndrome von CHESSA, L., BASTIANON, V., PORTO, G. DEL, NARDO, T., STEFANINI, M.

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Imbalance in the Antioxidant Pool in Melanoma Cells and Normal Melanocytes from Patients with Melanoma von Picardo, Mauro, Grammatico, Paola, Roccella, Francesca, Roccella, Maria, Grandinetti, Mauro, del Porto, Giuseppe, Passi, Siro

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Cytogenetic findings in 20 melanomas von Grammatico, P, Catricalà, C, Potenza, C, Amantea, A, Roccella, M, Roccella, F, Eibenschutz, L, Del Porto, G

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Chromosome heteromorphisms and early recurrent abortions von Porto, G. Del, D'Alessandro, E., Grammatico, P., Coghi, I.M., DeSanctis, S., Giambenedetti, M., Vaccarella, C., Fabi, R., Marcaino, M.F., Nicotra, M.

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6p23 Deletion mosaicism in a woman with recurrent abortions and idiopathic hypoprolactinemia von D'Alessandro, Elvira, Santiemma, Vittorio, Re, Maria Luisa Lo, Ligas, Claudio, Del Porto, Giuseppe

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Familial centric fission of chromosome 4 von Del Porto, G, Di Fusco, C, Baldi, M, Grammatico, P, D'Alessandro, E

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Familial paracentric inversion of chromosome 15 (q15q24) von Del Porto, G, D'Alessandro, E, De Matteis, C, D'Innocenzo, R, Baldi, M, Pachi, A, Cappa, F

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3p13 Region: A Possible Location of a Tumor Suppressor Gene Involved in Uveal Melanoma von Blasi, M.A., Roccella, F., Balestrazzi, E., Del Porto, G., De Felice, N., Roccella, M., Rota, R., Grammatico, P.

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Autosomal dominant simple microphthalmos von Vingolo, E M, Steindl, K, Forte, R, Zompatori, L, Iannaccone, A, Sciarra, A, Del Porto, G, Pannarale, M R

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Cytogenetic Follow-Up in a Case With a Primary Cutaneous Melanoma and Five Metastatic Lesions von GRAMMATICO, PAOLA, EIBENSCHUTZ, LAURA, ROCCELLA, FRANCESCA, AMANTEA, ADA, ROCCELLA, MARIA, CATRICALÀ, CATERINA, MICCI, FRANCESCA, PORTO, GIUSEPPE DEL

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