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Jaundice AND familial chronic idiopathic journal articles from PubMed MEDLINE database

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Jung MK, Bae MH, Kim DJ, et al. 
[A case with rotor syndrome in hyperbilirubinemic family.] [English Abstract, Journal Article]
Korean J Gastroenterol 2007 Apr; 49(4):251-5.
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Hrebícek M, Jirásek T, Hartmannová H, et al. 
Rotor-type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump. [Journal Article]
Liver Int 2007 May; 27(4):485-91.
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Silva LP, Queiros F, Lima I 
[Etiology of hearing impairment in children and adolescents of a reference center APADA in the city of Salvador, state of Bahia.] [Journal Article]
Rev Bras Otorrinolaringol (Engl Ed) 2006 Jan-Feb; 72(1):33-6.
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Jedlitschky G, Hoffmann U, Kroemer HK 
Structure and function of the MRP2 (ABCC2) protein and its role in drug disposition. [JOURNAL ARTICLE]
Expert Opin Drug Metab Toxicol 2006 Jun; 2(3):351-366.
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Fretzayas A, Kitsiou S, Papadopoulou A, et al. 
Clinical expression of co-inherited Dubin-Johnson and thalassaemic heterozygous states. [JOURNAL ARTICLE]
Dig Liver Dis 2006 Mar 21.
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Kubitz R, Keitel V, Häussinger D 
Inborn errors of biliary canalicular transport systems. [Journal Article, Review]
Methods Enzymol 2005.:558-69.
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Machida I, Wakusawa S, Sanae F, et al. 
Mutational analysis of the MRP2 gene and long-term follow-up of Dubin-Johnson syndrome in Japan. [Journal Article]
J Gastroenterol 2005 Apr; 40(4):366-70.
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Wakusawa S, Machida I, Suzuki S, et al. 
Identification of a novel 2026G-->C mutation of the MRP2 gene in a Japanese patient with Dubin-Johnson syndrome. [Case Reports, Journal Article]
J Hum Genet 2003; 48(8):425-9.
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Tate G, Li M, Suzuki T, et al. 
A new mutation of the ATP-binding cassette, sub-family C, member 2 (ABCC2) gene in a Japanese patient with Dubin-Johnson syndrome. [Case Reports, Journal Article]
Genes Genet Syst 2002 Apr; 77(2):117-21.
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Elferink RO, Groen AK 
Genetic defects in hepatobiliary transport. [Journal Article, Review]
Biochim Biophys Acta 2002 Mar 16; 1586(2):129-45.
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