المؤلفون: Pellegrini, Cristina, Botta, Francesca, Massi, Daniela, Martorelli, Claudia, Facchetti, Fabio, Gandini, Sara, Maisonneuve, Patrick, Avril, Marie-Françoise, Demenais, Florence, Paillerets, Brigitte Bressac-de, Hoiom, Veronica, Cust, Anne E, Anton-Culver, Hoda, Gruber, Stephen B, Gallagher, Richard P, Marrett, Loraine, Zanetti, Roberto, Dwyer, Terence, Thomas, Nancy E, Begg, Colin B, Berwick, Marianne, Puig, Susana, Potrony, Miriam, Nagore, Eduardo, Ghiorzo, Paola, Menin, Chiara, Manganoni, Ausilia Maria, Rodolfo, Monica, Brugnara, Sonia, Passoni, Emanuela, Sekulovic, Lidija Kandolf, Baldini, Federica, Guida, Gabriella, Stratigos, Alexandros, Ozdemir, Fezal, Ayala, Fabrizio, Fernandez-de-Misa, Ricardo, Quaglino, Pietro, Ribas, Gloria, Romanini, Antonella, Migliano, Emilia, Stanganelli, Ignazio, Kanetsky, Peter A, Pizzichetta, Maria Antonietta, García-Borrón, Jose Carlos, Nan, Hongmei, Landi, Maria Teresa, Little, Julian, Newton-Bishop, Julia, Sera, Francesco, Fargnoli, Maria Concetta, Raimondi, Sara, Group, IMI Study, Alaibac, Mauro, Ferrari, Andrea, Valeri, Barbara, Sicher, Mariacristina, Mangiola, Daniela, Nazzaro, Gianluca, Tosti, Giulio, Mazzarol, Giovanni, Giudice, Giuseppe, Ribero, Simone, Astrua, Chiara, Mazzoni, Laura, Group, GEM Study, Orlow, Irene, Mujumdar, Urvi, Hummer, Amanda, Busam, Klaus, Roy, Pampa, Canchola, Rebecca, Clas, Brian, Cotignola, Javiar, Monroe, Yvette, Armstrong, Bruce, Kricker, Anne, Litchfield, Melisa, Tucker, Paul, Stephens, Nicola, Switzer, Teresa, Theis, Beth, From, Lynn, Chowdhury, Noori, Vanasse, Louise, Purdue, Mark, Northrup, David, Rosso, Stefano, Sacerdote, Carlotta, Leighton, Nancy, Gildea, Maureen, Bonner, Joe, Jeter, Joanne, Klotz, Judith, Wilcox, Homer, Weiss, Helen, Millikan, Robert, Mattingly, Dianne, Player, Jon

المصدر: The Lancet Child & Adolescent Health. 3(5)

مصطلحات موضوعية: Clinical Research, Pediatric, Genetics, Prevention, Cancer, Adolescent, Adult, Aged, Biomarkers, Tumor, Case-Control Studies, Child, Female, Genetic Predisposition to Disease, Germ-Line Mutation, Humans, Logistic Models, Male, Melanoma, Middle Aged, Odds Ratio, Polymorphism, Genetic, Receptor, Melanocortin, Type 1, Retrospective Studies, Skin Neoplasms, IMI Study Group, GEM Study Group, M-SKIP Study Group

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4144d96wTest

المؤلفون: Bougeard, Gaëlle, Brugieres, Laurence, Chompret, Agnes, Gesta, Paul, Charbonnier, Francoise, Valent, Alexander, Martin, Cosette, Raux, Grégory, Feunteun, Jean, Bressac-De Paillerets, Brigitte, Frébourg, Thierry, Paillerets, Brigitte Bressac-De

المساهمون: Génomique et Médecine Personnalisée du Cancer et des Maladies Neuropsychiatriques (GPMCND), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Département de cancérologie de l'enfant et de l'adolescent [Gustave Roussy], Institut Gustave Roussy (IGR), CHG Niort, Département de biologie et pathologie médicales [Gustave Roussy], Génétique médicale et fonctionnelle du cancer et des maladies neuropsychiatriques, Normandie Université (NU), Génétique oncologique (GO - UMR 8125), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Diagnostic Moléculaire, Département de Biologie Clinique

المصدر: Oncogene
Oncogene, Nature Publishing Group, 2003, 22 (6), pp.840-846. ⟨10.1038/sj.onc.1206155⟩

مصطلحات موضوعية: Male, MESH: DNA Primers, Cancer Research, MESH: Sequence Analysis, DNA, endocrine system diseases, Sequence analysis, MESH: Pedigree, MESH: Genes, p53, Alu element, Locus (genetics), Biology, Germline, Li-Fraumeni Syndrome, 03 medical and health sciences, Exon, 0302 clinical medicine, stomatognathic system, Genetics, medicine, Humans, Genetic Predisposition to Disease, MESH: Li-Fraumeni Syndrome, Molecular Biology, Gene, neoplasms, DNA Primers, 030304 developmental biology, 0303 health sciences, MESH: Humans, MESH: Genetic Predisposition to Disease, Sarcoma, Sequence Analysis, DNA, Gene rearrangement, Genes, p53, medicine.disease, Molecular biology, MESH: Male, Pedigree, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Li–Fraumeni syndrome, MESH: Gene Deletion, 030220 oncology & carcinogenesis, MESH: Sarcoma, Female, MESH: Female, Gene Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc2bdc30970aef7baba6dc51e854d090Test
https://hal.archives-ouvertes.fr/hal-03106947Test