المؤلفون: Lorenza Pastorino, Virginia Andreotti, Bruna Dalmasso, Irene Vanni, Giulia Ciccarese, Mario Mandalà, Giuseppe Spadola, Maria Pizzichetta, Giovanni Ponti, Maria Tibiletti, Elena Sala, Maurizio Genuardi, Pietro Chiurazzi, Gabriele Maccanti, Siranoush Manoukian, Serena Sestini, Rita Danesi, Valentina Zampiga, Roberta La Starza, Ignazio Stanganelli, Alberto Ballestrero, Luca Mastracci, Federica Grillo, Stefania Sciallero, Federica Cecchi, Enrica Tanda, Francesco Spagnolo, Paola Queirolo, Italian Melanoma Intergroup (IMI), Alisa Goldstein, William Bruno, Paola Ghiorzo

المصدر: Cancers; Volume 12; Issue 4; Pages: 1007

مصطلحات موضوعية: familial melanoma, genetic susceptibility, gene panel sequencing, high-penetrance genes, variant interpretation, missing heritability, CDKN2A, ATM, BAP1, POT1

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/cancers12041007

الاتاحة: https://doi.org/10.3390/cancers12041007

المؤلفون: Paola Queirolo, Federica Cecchi, Francesco Spagnolo, Italian Melanoma Intergroup, Rita Danesi, Virginia Andreotti, Enrica Teresa Tanda, Giovanni Ponti, Paola Ghiorzo, Roberta La Starza, Siranoush Manoukian, Federica Grillo, Bruna Dalmasso, Pietro Chiurazzi, William Bruno, Maurizio Genuardi, Alisa M. Goldstein, Elena Sala, Valentina Zampiga, Giuseppe Spadola, Ignazio Stanganelli, Gabriele Maccanti, Luca Mastracci, Serena Sestini, Irene Vanni, Maria Grazia Tibiletti, Giulia Ciccarese, Lorenza Pastorino, Mario Mandalà, Alberto Ballestrero, Maria Antonietta Pizzichetta, Stefania Sciallero

المساهمون: L., Pastorino, V., Andreotti, B., Dalmasso, I., Vanni, G., Ciccarese, M., Mandala, G., Spadola, Pizzichetta, MARIA ANTONIETTA, G., Ponti, M., Grazia Tibiletti, E., Sala, M., Genuardi, P., Chiurazzi, G., Maccanti, S., Manoukian, S., Sestini, R., Danesi, V., Zampiga, R., La Starza, I., Stanganelli, A., Ballestrero, L., Mastracci, F., Grillo, S., Sciallero, F., Cecchi, E., Teresa Tanda, F., Spagnolo, P., Queirolo, A. M., Goldstein, W., Bruno, P., Ghiorzo

المصدر: Cancers
Volume 12
Issue 4
Cancers, Vol 12, Iss 1007, p 1007 (2020)

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Candidate gene, Population, Biology, Settore MED/03 - GENETICA MEDICA, ATM, BAP1, CDKN2A, POT1, familial melanoma, gene panel sequencing, genetic susceptibility, high-penetrance genes, missing heritability, variant interpretation, lcsh:RC254-282, High-penetrance gene, Article, Loss of heterozygosity, 03 medical and health sciences, 0302 clinical medicine, Missing heritability problem, Genetic susceptibility, melanoma, Genetic predisposition, education, neoplasms, Variant interpretation, Genetics, education.field_of_study, Gene panel sequencing, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Missing heritability, Familial melanoma, High-penetrance genes, Penetrance, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Cutaneous melanoma

وصف الملف: application/pdf; ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc242c0ce1ab9c1ac7b9de169c2891dc
https://hdl.handle.net/11391/1471312