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Issue Date | Title | Author(s) |
---|---|---|
11-Jan-2010 | Les xifres del tabac | Bueno i Torrens, David, 1965- |
14-Jun-2013 | Models in vivo i in vitro per a l'estudi de gens causants de distròfies de retina: CERKL i RP2. | Riera Gibernau, Marina |
13-Dec-2012 | Finding genes related to homologous recombination as modifiers of the number of dermal neurofibromas in neurofibromatosis type 1 patients / Estudi sobre la implicació dels gens de recombinació homòloga com a modificadors del nombre de neurofibromes dèrmics en pacients amb Neurofibromatosi tipus 1 | Garcia Linares, Carles |
17-Jul-2017 | Role of the Hippo pathway in planarians | Sousa, Nidia De |
Jun-2007 | Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene | Olivé i Plana, Montserrat; Armstrong i Morón, Judith; Miralles, Francesc; Pou, Adolf; Fardeau, Michel; González Mera, Laura; Martínez, Francesca; Fisher, Dirk; Martínez Matos, Juan Antonio; Shatunov, Alexey; Goldfarb, Lev G.; Ferrer, Isidro (Ferrer Abizanda) |
24-Jan-2017 | Activating mutations and translocations in the guanine exchange factor VAV1 in peripheral T-cell lymphomas. | Abate, Francesco; Silva-Almeida, Ana C. da; Zairis, Sakellarios; Robles Valero, Javier; Couronne, Lucile; Khiabanian, Hossein; Quinn, S. Aidan; Kim, Mi-Yeon; Laginestra, M.Antonella; Kim, Christine; Fiore, Danilo; Bhagat, Govind; Piris, Miguel A.; Campo Güerri, Elias; Lossos, Izidore S.; Bernard, Olivier A.; Inghirami, Giorgio; Pileri, Stefano Aldo; Bustelo, Xosé R.; Rabadán, Raul; Ferrando, Adolfo A.; Palomero, Teresa |
Jul-2016 | Identification of gene mutations and fusion genes in patients with Sézary Syndrome | Prasad, Aparna; Rabionet Janssen, Raquel; Espinet Solà, Blanca; Zapata, Luis; Puiggros Metje, Anna M.; Melero, Carme; Puig, Anna; Sarria Trujillo, Yaris; Ossowski, Stephan; Garcia-Muret, Maria P.; Estrach Panella, Ma. Teresa (María Teresa); Servitje Bedate, Octavio; Lopez Lerma, Ingrid; Gallardo, F. (Fernando); Pujol, Ramon M.; Estivill, Xavier, 1955- |
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