• 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