A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects. (1/10)

Effect of zoledronic acid on acro-osteolysis and osteoporosis in a patient with Hajdu-Cheney syndrome. (2/10)

Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndrome. (3/10)

Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME. (4/10)

Notch signaling in human development and disease. (5/10)

Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB. (6/10)

Particle disease: biologic mechanisms of periprosthetic osteolysis in total hip arthroplasty. (7/10)

Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome. (8/10)

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