Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families
Zachara, E, Caforio, A L, Carboni, G P, Pellegrini, A, Pompili, A, Del Porto, G, Sciarra, A, Bosman, C, Boldrini, R, Prati, P L
Published in British Heart Journal (01.02.1993)
Published in British Heart Journal (01.02.1993)
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Clinical management and molecular cytogenetic characterization in a 45,X/46,X,idic(Yp) patient with severe hypospadia
Marrocco, G, Poscente, M, Majore, S, De Bernardo, C, Rinaldi, R, Del Porto, G, Storniello, G, Grammatico, P
Published in Journal of pediatric surgery (01.08.2003)
Published in Journal of pediatric surgery (01.08.2003)
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Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis
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
Published in American journal of human genetics (01.02.1993)
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Published in American journal of human genetics (01.02.1993)
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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
Varesco, L, Gismondi, V, Presciuttini, S, Groden, J, Spirio, L, Sala, P, Rossetti, C, De Benedetti, L, Bafico, A, Heouaine, A
Published in Human genetics (01.03.1994)
Published in Human genetics (01.03.1994)
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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
PANNARALE, M. R, GRAMMATICO, B, IANNACCONE, A, FORTE, R, DE BERNARDO, C, FLAGIELLO, L, VINGOLO, E. M, DEL PORTO, G
Published in Ophthalmology (Rochester, Minn.) (01.09.1996)
Published in Ophthalmology (Rochester, Minn.) (01.09.1996)
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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
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
Published in Human mutation (1998)
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Published in Human mutation (1998)
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A low NM23.H1 gene expression identifying high malignancy human melanomas
Caligo, M A, Grammatico, P, Cipollini, G, Varesco, L, Del Porto, G, Bevilacqua, G
Published in Melanoma research (01.06.1994)
Published in Melanoma research (01.06.1994)
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Involvement of the 4q21 region in human malignant melanomas: cytogenetic and immunocytochemical characterization of three primary cell cultures
Grammatico, P, Roccella, M, Catricalà, C, Roccella, F, Bucher, S, Mordenti, C, Amantea, A, Di Rosa, C, Del Porto, G
Published in World journal of surgery (01.05.1995)
Published in World journal of surgery (01.05.1995)
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46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes
Grammatico, P, Majore, S, Marrocco, G, Poscente, M, Mordenti, C, Grammatico, B, Del Porto, G
Published in Genetic counseling (1999)
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Published in Genetic counseling (1999)
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Cytogenetic and DNA repair studies in a patient affected by the neonatal progeroid syndrome
Chessa, L, Bastianon, V, Del Porto, G, Nardo, T, Stefanini, M
Published in Annals of the New York Academy of Sciences (01.11.1992)
Published in Annals of the New York Academy of Sciences (01.11.1992)
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Variable number of tandem repeats in zygosity diagnosis in twins
Costanzi Porrini, S, Sciarra, A, Sulli, N, Piane, M, Gualtieri, R, Del Porto, G
Published in Acta geneticae medicae et gemellologiae (1990)
Published in Acta geneticae medicae et gemellologiae (1990)
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Del(4)(pter-->q33:) case report and review of the literature
Grammatico, P, Spaccini, L, Di Rosa, C, Cupilari, F, Del Porto, G
Published in Genetic counseling (1997)
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Published in Genetic counseling (1997)
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Inv dup(15): contribution to the clinical definition of phenotype
Grammatico, P, Di Rosa, C, Roccella, M, Falcolini, M, Pelliccia, A, Roccella, F, Del Porto, G
Published in Clinical genetics (01.09.1994)
Published in Clinical genetics (01.09.1994)
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2q35qter duplication syndrome: phenotypic definition
Grammatico, P, Di Rosa, C, Rinaldi, R, Roccella, M, Cupilari, F, Sbezzi, T, Del Porto, G
Published in Genetic counseling (1997)
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Published in Genetic counseling (1997)
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Chromosome heteromorphisms and early recurrent abortions
Del Porto, G, D'Alessandro, E, Grammatico, P, Coghi, I M, DeSanctis, S, Giambenedetti, M, Vaccarella, C, Fabi, R, Marcaino, M F, Nicotra, M
Published in Human reproduction (Oxford) (01.05.1993)
Published in Human reproduction (Oxford) (01.05.1993)
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A balanced complex chromosomal rearrangement (BCCR) with phenotypic effect
Del Porto, G, Grammatico, P, De Sanctis, S, Esposito, M, Di Rosa, C, Romano, C
Published in Clinical genetics (01.07.1991)
Published in Clinical genetics (01.07.1991)
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Cytogenetic findings in 20 melanomas
Grammatico, P, Catricalà, C, Potenza, C, Amantea, A, Roccella, M, Roccella, F, Eibenschutz, L, Del Porto, G
Published in Melanoma research (01.06.1993)
Published in Melanoma research (01.06.1993)
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