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胆管板畸形与先天性胆管发育异常 被引量:1

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出处 《肝胆外科杂志》 2001年第4期316-318,共3页 Journal of Hepatobiliary Surgery
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  • 1[1]Desmet VJ.Ludwig symposium on biliary disorders-part Ⅰ.Pathogenesis of ductal plate abnormalities.Mayo Clin Proc,1998,73(1):80-89.
  • 2[2]Zerres K,Mucher G,Becker J,et al.Prenatal diagnosis of autosomal recessive polycystic kidney disease(ARPKD):molecular genetics,clinical experience,and fetal morphology.Am J Med Genet,1998,76(2):137-144.
  • 3[3]Fabris L,Strazzabosco M,Crosby HA,et al.Characterization and isolation of ductular cells coexpressing neural cell adhesion molecule and Bcl-2 from primary cholangiopathies and ductal plate malformation.Am J Pathol,2000,156(5):1599-1612.
  • 4[4]Sergi C,Kahl P,Otto HF.Contribution of apoptosis and apoptosis-related protein to the malformation of the primitive intrahepatic biliary system in Mechel syndrome.Am J Pathol,2000,156(5):1589-1598.
  • 5[5]Vijayan V,Tan CE.Cmputer-generated three-dimensional morphology of the hepatic hilar bile ducts in biliary atresia.J Pediatr Surg,2000,35(8):1230-1235.

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