Disease: Osteosclerosis autosomal dominant Worth type
- A Mild Case of Autosomal Recessive Osteopetrosis Masquerading as the Dominant Form Involving Homozygous Deep Intronic Variations in the CLCN7 Gene
- Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease models
- Genotyping, generation and proteomic profiling of the first human autosomal dominant osteopetrosis type II-specific induced pluripotent stem cells
- LRP5 high bone mass (Worth-type autosomal dominant endosteal hyperostosis): case report and historical review of the literature
- Worth syndrome as a diagnosis for mandibular osteosclerosis