Author:
Phadke Shubha R.,Ramirez Maria,DiFeo Analisa,Martignetti John A.,Girisha Katta M.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Al-Aqeel Sewari syndrome, a new autosomal recessive disorder with multicentric osteolysis, nodulosis and arthropathy. The first genetic disorder of matrix metalloproteinase 2 gene;Al-Aqeel;Saudi Med J,2005
2. New form of idiopathic osteolysis: nodulosis, arthropathy and osteolysis (NAO) syndrome;Al-Mayouf;Am J Med Genet,2000
3. Beneficial effects of biphosphonates during five years of treatment of severe osteogenesis imperfecta;Astrom;Acta Paediatr,1998
4. Torg osteolysis syndrome;Eisenstein;Am J Med Genet,1998
5. Cyclic administration of pamidronate in children with severe osteogenesis imperfecta;Glorieux;N Engl J Med,1998
Cited by
12 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献