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致密性成骨不全1例报道 被引量:3

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出处 《中国矫形外科杂志》 CAS CSCD 北大核心 2007年第21期1674-1674,共1页 Orthopedic Journal of China
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  • 2Glorieux FH,Ward LM,Rauch F,et al. Osteogenesis imperfecta type Ⅵ: a form of brittle bone disease with a mineralization defect [J]. J Bone Miner Res ,2002,17:30-38. 被引量:1
  • 3Ward LM, Rauch F, Travers R, et al. Osteogenesis imperfecta type Ⅶ:an autosomal recessive form of brittle bone disease [J]. Bone,2002,31:12-18. 被引量:1
  • 4Rauch F,Travers R,Parfitt AM,et al. Static and dynamic bone histomorphometry in children with osteogenesis imperfecta [J]. Bone,2000,26:581-589. 被引量:1
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  • 6Jones S J,Glorieux FH,Travers R,et al. The microscopic structure of bone in normal children and patients with osteogenesis imperfecta: A survey using backscattered electron imaging [J]. Calcif Tissue Int,1999,64:8-17. 被引量:1
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  • 9Plotkin H, Rauch F, Bishop NJ, et al. Pamidronate treatment of seve re osteogenesis imperfecta in children under 3 years of age [J]. J Clin Endocrinol Metab,2000,85:1846-1850. 被引量:1
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共引文献10

同被引文献78

  • 1林贞鼎,游斌.致密性成骨不全x线诊断(附1例报告)[J].中国罕少见病杂志,1995,2(1):46-46. 被引量:2
  • 2杨增敏,吴莹.致密性成骨不全症1例报告[J].中医正骨,2007,19(8):15-15. 被引量:3
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  • 6Fleming KW,Barest G,Sakai O.Dental and facial bone abnormalities in pyknodysostosis:CT findings.AJNR Am J Neuroradiol,2007,28 (1):132-134. 被引量:1
  • 7Gelb BD,Moissoglu K,Zhang J,et al.Cathepsin K:isolation and characterization of the murine cDNA and genomic sequence,the homologue of the human pycnodysostosis gene.Biochem Mol Med,1996,59(2):200-206. 被引量:1
  • 8Polymeropoulos MH,Ortiz De Luna RI,Ide SE,et al.The gene for pycnodysostosis maps to human chromosome 1cen-q21.Nat Genet,1995,10 (2):238-239. 被引量:1
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