Navegação por autor "Hoischen, Alexander"
Itens para a visualização no momento 1-2 of 2
-
DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome
White, Janson et al. | Data do documento: 2015 -
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies
Acuna-Hidalgo, Rocio et al. | Data do documento: 2017