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Journal Abstract Search

137 related items for PubMed ID: 2353208

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  • 3. Familial expansile osteolysis. A new dysplasia.
    Osterberg PH, Wallace RG, Adams DA, Crone RS, Dickson GR, Kanis JA, Mollan RA, Nevin NC, Sloan J, Toner PG.
    J Bone Joint Surg Br; 1988 Mar; 70(2):255-60. PubMed ID: 3346299
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  • 4. Familial expansile osteolysis.
    Wallace RG, Barr RJ, Osterberg PH, Mollan RA.
    Clin Orthop Relat Res; 1989 Nov; (248):265-77. PubMed ID: 2530018
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  • 5. Familial expansile osteolysis: An Australian case report of a Paget's Disease Mimic.
    Topham DG, Sampson MJ.
    J Med Imaging Radiat Oncol; 2016 Jun; 60(3):370-3. PubMed ID: 27258166
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  • 7. Expansile bone lesions in a three-generation family.
    Dinulos MB, Sternen DL, Graham CB, Hudgins L.
    Am J Med Genet; 1999 Jan 01; 82(1):1-5. PubMed ID: 9916834
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  • 8. Progressive facial disfigurement and deafness in craniometaphyseal dysplasia.
    Vasu CK, Rajendran VR, Regi George AN, Anoop P, Anjay MA.
    Indian J Pediatr; 2006 Dec 01; 73(12):1105. PubMed ID: 17202639
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  • 9. Gorham's massive osteolysis of the mandible - a progressive radiographic presentation.
    Raghuveer HP, Jayalekshmy R.
    Dentomaxillofac Radiol; 2009 Jul 01; 38(5):292-5. PubMed ID: 19474257
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  • 10. Hereditary osteodysplasia with acro-osteolysis. (The Hajdu-Cheney syndrome).
    Elias AN, Pinals RS, Anderson HC, Gould LV, Streeten DH.
    Am J Med; 1978 Oct 01; 65(4):627-36. PubMed ID: 707523
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  • 11. Identification of a novel tandem duplication in exon 1 of the TNFRSF11A gene in two unrelated patients with familial expansile osteolysis.
    Johnson-Pais TL, Singer FR, Bone HG, McMurray CT, Hansen MF, Leach RJ.
    J Bone Miner Res; 2003 Feb 01; 18(2):376-80. PubMed ID: 12568416
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  • 12. [Hereditary multicentric osteolysis].
    Addor MC, Pescia G, Egloff D, Quéloz J.
    J Genet Hum; 1986 Aug 01; 34(3-4):293-303. PubMed ID: 3760832
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  • 13. Acromesomelic dysplasia.
    Langer LO, Garrett RT.
    Radiology; 1980 Nov 01; 137(2):349-55. PubMed ID: 7433666
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  • 14. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.
    Whyte MP.
    Ann N Y Acad Sci; 2006 Apr 01; 1068():143-64. PubMed ID: 16831914
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  • 17. Hyperphosphatasemia: report of three cases.
    Bonakdarpour A, Maldjian C, Weiss S, Roach N, Stein E.
    Eur J Radiol; 2000 Jul 01; 35(1):54-8. PubMed ID: 10930767
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  • 19. Frontometaphyseal dysplasia: autosomal dominant or X-linked?
    Beighton P, Hamersma H.
    J Med Genet; 1980 Feb 01; 17(1):53-6. PubMed ID: 7189217
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