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Journal Article

Catucci, Irene, Osorio, Ana ORCID: 0000-0001-8124-3984, Arver, Brita, Neidhardt, Guido, Bogliolo, Massimo ORCID: 0000-0001-8240-7784, Zanardi, Federica, Riboni, Mirko, Minardi, Simone, Pujol, Roser, Azzollini, Jacopo ORCID: 0000-0002-9364-9778, Peissel, Bernard, Manoukian, Siranoush, De Vecchi, Giovanna, Casola, Stefano ORCID: 0000-0001-5580-0986, Hauke, Jan, Richters, Lisa, Rhiem, Kerstin, Schmutzler, Rita K., Wallander, Karin ORCID: 0000-0001-8166-9678, Torngren, Therese, Borg, Ake, Radice, Paolo ORCID: 0000-0001-6298-4111, Surralles, Jordi, Hahnen, Eric, Ehrencrona, Hans ORCID: 0000-0002-5589-3622, Kvist, Anders ORCID: 0000-0002-1358-0695, Benitez, Javier and Peterlongo, Paolo ORCID: 0000-0001-6951-6855 (2018). Individuals with &ITFANCM&IT biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility. Genet. Med., 20 (4). S. 452 - 458. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1530-0366

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