Genetic and biochemical study of dual hereditary jaundice: Dubin–Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2

Lignende værker

• Genetic and biochemical study of dual hereditary jaundice: Dubin–Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2
  af: Slachtova, Lenka, et al.
  Udgivet: (2016)
• Porphyrin metabolism in Gilbert's, Dubin-Johnson, and Rotor's syndromes.
  af: Mikulecký, M
  Udgivet: (1987)
• Mutation analysis of the ABCC2 gene in Chinese patients with Dubin-Johnson syndrome
  af: Wu, Lina, et al.
  Udgivet: (2018)
• Chronic Idiopathic Jaundice with Unidentified Pigment in Liver Cells (Dubin-Johnson Syndrome)
  af: Halpenny, G. W., et al.
  Udgivet: (1957)
• Intractable neonatal jaundice due to hereditary spherocytosis and Gilbert’s syndrome
  af: Ismail, Abdul Qader Tahir, et al.
  Udgivet: (2011)