An unusual phenotype of MEN1 syndrome with a SI-NEN associated with a deletion of the MEN1 gene

by Manoharan, Jerena, Lopez, Caroline L, Hackmann, Karl, Albers, Max B, Pehl, Anika, Kann, Peter H, Slater, Emily P, Schröck, Evelin, Bartsch, Detlef K
Published 2016