Stephen J Marx

Mutations in CDKN2C (p18) and CDKN2D (p19) may cause sporadic parathyroid adenoma.

Ziqiang Yuan, Thomas Gluick, S. Libutti, 2013, Endocrine-related cancer.

Impaired cotranslational processing of the calcium-sensing receptor due to signal peptide missense mutations in familial hypocalciuric hypercalcemia.

W. Simonds, G. Hendy, S. Marx, 2005, Human molecular genetics.

Genome-Wide Analysis of Menin Binding Provides Insights into MEN1 Tumorigenesis

Sean Davis, Francis S Collins, Peter C Scacheri, 2006, PLoS genetics.