Neurofibromatosis type 1 is a genetic skeletal disorder
- 13 August 2007
- journal article
- other
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 143A (17), 2082-2083
- https://doi.org/10.1002/ajmg.a.31758
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Neurofibromatosis UpdateJournal of Pediatric Orthopaedics, 2006
- Decreased bone mineral density and content in neurofibromatosis type 1: Lowest local values are located in the load-carrying parts of the bodyOsteoporosis International, 2004
- NF1 Tumor Suppressor Protein and mRNA in Skeletal Tissues of Developing and Adult Normal Mouse and NF1-Deficient EmbryosJournal of Bone and Mineral Research, 2004
- Decreased Bone Mineral Density in Neurofibromatosis-1 Patients with Spinal DeformitiesOsteoporosis International, 2001
- Modulation of Spinal Deformities in Patients With Neurofibromatosis Type 1Spine, 2000
- Neurofibromatosis in Children: The Role of the OrthopaedistJournal of the American Academy of Orthopaedic Surgeons, 1999
- The Management of Scoliosis in NeurofibromatosisSpine, 1997
- The Diagnostic Evaluation and Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2JAMA, 1997
- A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutationsCell, 1990
- Osseous Manifestations of Neurofibromatosis in ChildhoodJournal of Pediatric Orthopaedics, 1986