المؤلفون: Ciccarese G., Dalmasso B., Bruno W., Queirolo P., Pastorino L., Andreotti V., Spagnolo F., Tanda E., Ponti G., Massone C., Drago F., Parodi A., Ghigliotti G., Pizzichetta M. A., Ghiorzo P.

المساهمون: Ciccarese, G., Dalmasso, B., Bruno, W., Queirolo, P., Pastorino, L., Andreotti, V., Spagnolo, F., Tanda, E., Ponti, G., Massone, C., Drago, F., Parodi, A., Ghigliotti, G., Pizzichetta, M. A., Ghiorzo, P.

مصطلحات موضوعية: Cancer genetic, Cutaneous melanoma, Dermoscopy, Dysplastic nevi, E318K, Germline variant, Melanocyte Inducing Transcription Factor, Nevi, Renal cell carcinoma, Susceptibility

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32054529; info:eu-repo/semantics/altIdentifier/wos/WOS:000515849900001; volume:18; firstpage:78; lastpage:89; numberofpages:12; journal:JOURNAL OF TRANSLATIONAL MEDICINE; https://hdl.handle.net/11567/1009814Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85079334638

الإتاحة: https://doi.org/10.1186/s12967-020-02253-8Test
https://hdl.handle.net/11567/1009814Test

المؤلفون: Manca A., Paliogiannis P., Colombino M., Casula M., Lissia A., Botti G., Caraco C., Ascierto P. A., Sini M. C., Palomba G., Pisano M., Dedola M. F., Fedeli M. A., Montesu M. A., Rubino C., Satta R., Scotto T., Sini G., Maio M., Massi D., Anichini A., Pfeffer U., Doneddu V., Cossu A., Palmieri G., Ghiorzo P., Queirolo P., Quaglino P., Sileni V. C., Di Giacomo A. M.

المساهمون: Manca, A., Paliogiannis, P., Colombino, M., Casula, M., Lissia, A., Botti, G., Caraco, C., Ascierto, P. A., Sini, M. C., Palomba, G., Pisano, M., Dedola, M. F., Fedeli, M. A., Montesu, M. A., Rubino, C., Satta, R., Scotto, T., Sini, G., Maio, M., Massi, D., Anichini, A., Pfeffer, U., Doneddu, V., Cossu, A., Palmieri, G., Ghiorzo, P., Queirolo, P., Quaglino, P., Sileni, V. C., Di Giacomo, A. M.

مصطلحات موضوعية: BRAF, Cancer, Melanoma, Metastasi, Mutation, NRAS, Skin

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31455347; info:eu-repo/semantics/altIdentifier/wos/WOS:000483363300004; volume:17; firstpage:289; lastpage:298; numberofpages:10; journal:JOURNAL OF TRANSLATIONAL MEDICINE; http://hdl.handle.net/11567/971741Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85071640531

الإتاحة: https://doi.org/10.1186/s12967-019-2039-4Test
http://hdl.handle.net/11567/971741Test

المؤلفون: Borghesi, Alessandro, Mencarelli, Maria Antonietta, Memo, Luigi, Ferrero, Giovanni Battista, Bartuli, Andrea, Genuardi, Maurizio, Stronati, Mauro, Villani, Alberto, Renieri, Alessandra, Corsello, GiovanniAgostiniani R, Staiano A, Del Vecchio A, Banderali G, Peroni D, Piazzolla R, Turra R, Bozzola E, Vecchio D, Rosati GV, Macrì F, Romagnoli C, De Curtis M, Orfeo L, Mangili G, Mosca F, Fanos V, Paolillo P, Raimondi F, Rizzo A, Chirico G, Corvaglia LT, Cacace C, Poggiani C, Zuppa AA, Pisano D, Melis D, Giuffrè M, Carbone MT, Macchiaiolo M, Tarani L, Selicorni A, Andria G, Coviello D, Gentile M, Ghiorzo P, Novelli A, Ragusa A, Scarano G, Giardino D.

المساهمون: Borghesi, Alessandro, Mencarelli, Maria Antonietta, Memo, Luigi, Ferrero, Giovanni Battista, Bartuli, Andrea, Genuardi, Maurizio, Stronati, Mauro, Villani, Alberto, Renieri, Alessandra, Corsello, Giovanniagostiniani, R, Staiano, A, Del Vecchio, A, Banderali, G, Peroni, D, Piazzolla, R, Turra, R, Bozzola, E, Vecchio, D, Rosati, Gv, Macrì, F, Romagnoli, C, De Curtis, M, Orfeo, L, Mangili, G, Mosca, F, Fanos, V, Paolillo, P, Raimondi, F, Rizzo, A, Chirico, G, Corvaglia, Lt, Cacace, C, Poggiani, C, Zuppa, Aa, Pisano, D, Melis, D, Giuffrè, M, Carbone, Mt, Macchiaiolo, M, Tarani, L, Selicorni, A, Andria, G, Coviello, D, Gentile, M, Ghiorzo, P, Novelli, A, Ragusa, A, Scarano, G, Giardino, D.

مصطلحات موضوعية: Diagnosi, Genetic, Genome, Mendelian, Neonatal intensive care unit, Neonate, NICU, WES, WGS, Whole-exome sequencing, Pediatrics, Perinatology and Child Health

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29100554; info:eu-repo/semantics/altIdentifier/wos/WOS:000414583600001; volume:43, fasc. 1, Article number 100; firstpage:1; lastpage:8; numberofpages:8; journal:THE ITALIAN JOURNAL OF PEDIATRICS; http://hdl.handle.net/11567/884626Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85032816868

الإتاحة: https://doi.org/10.1186/s13052-017-0418-0Test
http://hdl.handle.net/11567/884626Test

المؤلفون: Fargnoli M. C., Peris K.

المساهمون: Kim, J., Luo, W., Wang, M., Wegman-Ostrosky, T., Frone, M. N., Johnston, J. J., Nickerson, M. L., Rotunno, M., Li, S. A., Achatz, M. I., Brodie, S. A., Dean, M., De Andrade, K. C., Fortes, F. P., Gianferante, M., Khincha, P., Mcmaster, M. L., Mcreynolds, L. J., Pemov, A., Pinheiro, M., Santiago, K. M., Alter, B. P., Caporaso, N. E., Gadalla, S. M., Goldin, L. R., Greene, M. H., Loud, J., Yang, X. R., Freedman, N. D., Gapstur, S. M., Gaudet, M. M., Calista, D., Ghiorzo, P., Fargnoli, Maria Concetta, Nagore, E., Peris, Ketty, Puig, S., Landi, M. T., Hicks, B., Zhu, B., Liu, J., Sampson, J. N., Chanock, S. J., Mirabello, L. J., Morton, L. M., Biesecker, L. G., Tucker, M. A., Savage, S. A., Goldstein, A. M., Stewart, D. R.

مصطلحات موضوعية: ACMG secondary findings, Familial cancer exome, Population study, Variant classification, Aged, Cohort Studies, DNA Mutational Analysis, Ethnic Groups, Female, Genes, Neoplasm, Humans, Male, Neoplasms, Genetic Predisposition to Disease, Mutation, Polymorphism, Single Nucleotide, Settore MED/35 - MALATTIE CUTANEE E VENEREE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30583724; info:eu-repo/semantics/altIdentifier/wos/WOS:000454254400001; volume:10; issue:1; firstpage:99; lastpage:N/A; issueyear:2018; journal:GENOME MEDICINE; http://hdl.handle.net/10807/167432Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85058913898

الإتاحة: https://doi.org/10.1186/s13073-018-0607-5Test
http://hdl.handle.net/10807/167432Test