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Skeletal Radiology|October 2, 2003
Van Buchem disease: lifetime evolution of radioclinical featuresFilip M Vanhoenacker, Wendy Balemans, Gregorius J Tan, et al.
Seminars in Musculoskeletal Radiology|April 15, 2016
The Anterolateral Ligament of the Knee: What the Radiologist Needs to KnowPieter Van Dyck, Eline De Smet, Valérie Lambrecht, et al.
The Journal of Clinical Endocrinology and Metabolism|December 13, 2003
Patients with Van Buchem disease, an osteosclerotic genetic disease, have elevated bone formation markers, higher bone density, and greater derived polar moment of inertia than normalJon E Wergedal, Katarina Veskovic, Minea Hellan, et al.
Seminars in Musculoskeletal Radiology|April 15, 2016
Imaging of the Postoperative Anterior Cruciate Ligament: Emphasis on New Surgical and Imaging MethodsPieter Van Dyck, Valérie Lambrecht, Eline De Smet, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2015
Novel mutation in the BMPR1B gene (R486L) in a Polish family and further delineation of the phenotypic features of BMPR1B-related brachydactylyMagdalena Badura-Stronka, Dariusz Mróz, Peter Beighton, et al.
European Journal of Medical Genetics|July 9, 2017
SMD Kozlowski type caused by p.Arg594His substitution in TRPV4 reveals abnormal ossification and notochordal remnants in discs and vertebraeTadeusz Bieganski, Peter Beighton, Maciej Lukaszewski, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 3, 2015
Identification of a mutation in the ubiquitin-fold modifier 1-specific peptidase 2 gene, UFSP2, in an extended South African family with Beukes hip dysplasiaChristopher Mark Watson, Laura A Crinnion, Lindsay Gleghorn, et al.
Seminars in Musculoskeletal Radiology|October 10, 2023
Results of an International Survey on Spinal Imaging by the ASNR/ASSR/ESNR/ESSR "Nomenclature 3.0" Working GroupGennaro D'Anna, Lubdha Shah, Peter G Kranz, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|May 12, 2017
Osteogenesis imperfecta type 3 in South Africa: Causative mutations in FKBP10Alvera Vorster, Peter Beighton, Manogari Chetty, et al.
The Journal of Clinical Endocrinology and Metabolism|September 29, 2005
Bone mineral density in sclerosteosis; affected individuals and gene carriersJessica C Gardner, Rutger L van Bezooijen, Benjamin Mervis, et al.
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