Missense mutation in exon 7 of TRPS1 gene in an Italian family with a mild form of trichorhinophalangeal syndrome type I
Rossi, A., Devirgiliis, V., Panasiti, V., Borroni, R.G., Carlesimo, M., Gentile, M., Cariola, F., Calvieri, S.
Published in British journal of dermatology (1951) (01.11.2007)
Published in British journal of dermatology (1951) (01.11.2007)
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Holt–Oram syndrome associated with anomalies of the feet
Garavelli, L., De Brasi, D., Verri, R., Guareschi, E., Cariola, F., Melis, D., Calcagno, G., Salvatore, F., Unger, S., Sebastio, G., Albertini, G., Rivieri, F., Soli, F., Superti‐Furga, A., Gentile, M.
Published in American journal of medical genetics. Part A (01.05.2008)
Published in American journal of medical genetics. Part A (01.05.2008)
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Lapine rotaviruses of the genotype P[22] are widespread in Italian rabbitries
Martella, V., Ciarlet, M., Lavazza, A., Camarda, A., Lorusso, E., Terio, V., Ricci, D., Cariola, F., Gentile, M., Cavalli, A., Camero, M., Decaro, N., Buonavoglia, C.
Published in Veterinary microbiology (30.11.2005)
Published in Veterinary microbiology (30.11.2005)
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Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation
Buonadonna, A.L., Cariola, F., Caroppo, E., Carlo, A.Di, Fiorente, P., Valenzano, M.C., D'Amato, G., Gentile, M.
Published in Human reproduction (Oxford) (01.03.2002)
Published in Human reproduction (Oxford) (01.03.2002)
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A novel mutation in exon 7 in a family with mild tricho-rhino-phalangeal syndrome type I
Gentile, M, Fiorente, P, Buonadonna, A L, Macina, F, Cariola, F
Published in Clinical genetics (01.02.2003)
Published in Clinical genetics (01.02.2003)
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Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication
Gentile, M., Wuyts, W., Grittani, S., Di Carlo, A., Cariola, F., Verdyck, P., Margari, L., Perniola, T., Buonadonna, A.L.
Published in American journal of medical genetics. Part A (01.06.2004)
Published in American journal of medical genetics. Part A (01.06.2004)
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FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II
Gentile, M., De Sanctis, S., Cariola, F., Spezzi, T., Di Carlo, A., Tontoli, F., Lista, F., Buonadonna, A.L.
Published in European journal of medical genetics (2005)
Published in European journal of medical genetics (2005)
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Nine novel APC mutations in Italian FAP patients
Resta, N., Stella, A., Susca, F., Montera, M., Gentile, M., Cariola, F., Prete, F., Tenconi, R., Tibiletti, M.G., Logrieco, G., Mattina, T., Andriulli, G., Caruso, M.L., Fiorente, P., Russo, S., Caputi-Jambrenghi, O., Mareni, C., Guanti, G.
Published in Human mutation (01.05.2001)
Published in Human mutation (01.05.2001)
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Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14)
Gentile, Mattia, Buonadonna, Antonia L, Cariola, Filomena, Fiorente, Paola, Valenzano, Maria C, Guanti, Ginevra
Published in Journal of medical genetics (01.01.1999)
Published in Journal of medical genetics (01.01.1999)
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Eficacia de los sitios webs como herramienta comunicacional de los Diputados chilenos
Fuente-Alba Cariola, Fernando, Parada Gavilán, Carolina
Published in Revista de Comunicación (Peru) (26.08.2019)
Published in Revista de Comunicación (Peru) (26.08.2019)
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Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis
GUANTI, G, RESTA, N, SIMONE, C, CARIOLA, F, DEMMA, I, FIORENTE, P, GENTILE, M
Published in Human molecular genetics (22.01.2000)
Published in Human molecular genetics (22.01.2000)
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FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II
GENTILE, M, DESANCTIS, S, CARIOLA, F, SPEZZI, T, DICARLO, A, TONTOLI, F, LISTA, F, BUONADONNA, A
Published in Annales de génétique (07.12.2004)
Published in Annales de génétique (07.12.2004)
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Prenatal diagnosis of chromosome 4 mosaicism: Prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization
Gentile, Mattia, Volpe, Paolo, Cariola, Filomena, Carlo, Antonio Di, Marotta, Vincenzo, Buonadonna, Antonia Lucia, Boscia, Filippo Maria
Published in American journal of medical genetics. Part A (01.07.2005)
Published in American journal of medical genetics. Part A (01.07.2005)
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Oestrogen receptors and microsatellite instability in colorectal carcinoma patients
Notarnicola, Maria, Gristina, Roberto, Messa, Caterina, Cariola, Filomena, Fiorente, Paola, Caruso, Maria Lucia, Gentile, Mattia, Di Leo, Alfredo
Published in Cancer letters (10.07.2001)
Published in Cancer letters (10.07.2001)
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Reproductive genetics. Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation
Buonadonna, A L, Cariola, F, Caroppo, E, A.Di Carlo, Fiorente, P, Valenzano, M C, D'Amato, G, Gentile, M
Published in Human reproduction (Oxford) (01.03.2002)
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Published in Human reproduction (Oxford) (01.03.2002)
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Low presence of p53 abnormalities in H pylori-infected gastric mucosa and in gastric adenocarcinoma
Berloco, Pasquale, Russo, Francesco, Cariola, Filomena, Gentile, Mattia, Giorgio, Piero, Caruso, Maria Lucia, Valentini, Anna Maria, Di Matteo, Giovanni, Di Leo, Alfredo
Published in Journal of gastroenterology (2003)
Published in Journal of gastroenterology (2003)
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1 P P53 detection in gastric cancer: Comparison of immunohistochemistry, PCR/SSCP and DNA sequencing methods
Berloco, P., Russo, F., Notarnicola, M., Cavallini, A., Caruso, M.L., Valentini, A.M., Gentile, M., Cariola, F., Di Leo, A.
Published in Digestive and liver disease (01.06.2002)
Published in Digestive and liver disease (01.06.2002)
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The familial adenomatous polyposis region exhibits many different haplotypes
STELLA, A, RESTA, N, TIBILETTI, M. G, IZZO, P, GENTILE, M, PRETE, F, PANNARALE, O, DI MATTEO, G, SALA, P, VARESCO, L, MARENI, C, GUANTI, G, POLIZZI, A, MONTERA, M, CARIOLA, F, SUSCA, F, GISMONDI, V, BERTARIO, L, MARCHESE, C, TENCONI, R
Published in Human genetics (01.06.1998)
Published in Human genetics (01.06.1998)
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