Disease: Potter syndrome dominant type
- A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping
- A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (<em>NFIX</em>) Gene Has Phenotypic Features of Marshall-Smith Syndrome
- Angiotensin type I receptor blockade in conjunction with enhanced Akt activation restores coronary collateral growth in the metabolic syndrome
- Cannabis cultivation: Methodological issues for obtaining medical-grade product
- Computational study of biomechanical drivers of renal cystogenesis
- Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis
- Genetic aspects of uveal melanoma: a brief review
- Genetic etiology of renal agenesis: fine mapping of Renag1 and identification of Kit as the candidate functional gene
- Malignant fibrous histiocytoma of the lung
- Smad4 signalling in T cells is required for suppression of gastrointestinal cancer
- Transposition of anomalous left vertebral to carotid artery during the management of thoracic aortic dissections and aneurysms