Cancer Genet

Lynch syndrome and Muir-Torre phenotype associated with a recurrent variant in the 3'UTR of the MSH6 gene.

Cini G, Carnevali I, Sahnane N, ..., Viel A, Tibiletti MG

Cancer Genet 254-255 (-) 1-10 [2021-06-00; online 2021-01-19]

Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin.

Xochelli A, Baliakas P, Moore S, ..., Oscier D, Stamatopoulos K

Cancer Genet 207 (6) 281-283 [2014-06-00; online 2014-06-25]