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Autor:
Fagerholm, Rainer, Faltinova, Maria, Aaltonen, Kirsi, Aittomäki, Kristiina, Heikkilä, Päivi, Halttunen-Nieminen, Mervi, Nevanlinna, Heli, Blomqvist, Carl
Publikováno v:
Familial Cancer; Jul2018, Vol. 17 Issue 3, p321-331, 11p
Publikováno v:
Familial Cancer; Jul2017, Vol. 16 Issue 3, p339-349, 11p
Autor:
Walker, Meghan, Mirea, Lucia, Cooper, Kristine, Nabavi, Mitra, Glendon, Gord, Andrulis, Irene, Knight, Julia, O'Malley, Frances, Chiarelli, Anna
Publikováno v:
Familial Cancer; Jun2014, Vol. 13 Issue 2, p163-172, 10p
Publikováno v:
Familial Cancer; Nov2006, Vol. 5 Issue 4, p309-321, 13p
Autor:
Fabio Corradini, Francesco Piva, Riccardo Cellerino, C. Brugiati, R. Bracci, Eva Galizia, Italo Bearzi, Alessandra Viel, L. Belvederesi, Diana Baralle, Francesca Bianchi, Michela Raponi, Cristian Loretelli
Publikováno v:
Familial Cancer
Single base substitutions can lead to missense mutations, silent mutations or intronic mutations, whose significance is uncertain. Aberrant splicing can occur due to mutations that disrupt or create canonical splice sites or splicing regulatory seque