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Klippel-Feil综合征研究进展 被引量:6

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作者 刘洋 李明
出处 《脊柱外科杂志》 2005年第1期43-46,共4页 Journal of Spinal Surgery
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参考文献11

  • 1R. A. Clarke,Gale Catalan,Ashish D. Diwan,John H. Kearsley.Heterogeneity in Klippel-Feil syndrome: a new classification[J].Pediatric Radiology.1998(12)
  • 2Herman MJ,Pizzutillo PD.Cervical spine disorders in children[].Orthopedic Clinics of North America.1999
  • 3Theiss SM,Smith MD,Winter RB.The long term follow -up of patients with Klippel -Feil syndrome and congenital scoliosis[].SPINE.1997
  • 4Rouvreau P,Glorion C,Langlais J,et al.Assessment and neurologic involvement of patients with cervical spine congenital synostosis as in Klippel -Feil syndrome: Study of 19 cases[].Journal of Pediatric Orthopaedics.1998
  • 5Lander ES,Linton LM.Birren B et al: Initial sequencing and analysis of the human genome[].Nature.2001
  • 6Clarke RA,Kearsley JH,Walsh DA.Patterned expression in familial Klippel -Feil syndrome[].Teratology.1996
  • 7Li L,Krantz ID,Deng Y,et al.Alagille syndrome is caused by mutations in human Jagged 1 , which encodes a ligand for Notch 1[].Nature Genetics.1997
  • 8Chi N,Epstein JA.Getting your Pax straight: Pax proteins in development and disease[].Trends in Genetics.2002
  • 9Larson AR,Josephson KD,Pauli RM,et al.Klippel -Feil anomaly with Sprengel anomaly, omovertebral bone, thumb abnormalities, and flexion -crease changes: Novel association or syndrome[].American Journal of Medical Genetics.2001
  • 10Lowry RB,Jabs EW,Graham GE,et al.Syndrome of coronal craniosynostosis, Klippel -Feil anomaly, and Sprengel shoulder with and without Pro250 Arg mutation in the FGFR3 gene[].American Journal of Medical Genetics.2001

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二级引证文献9

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