These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
37. [Hyperbilirubinemia]. Thaler H Wien Med Wochenschr; 1972 Jan; 122(3):34-7. PubMed ID: 5060362 [No Abstract] [Full Text] [Related]
38. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Bull LN; van Eijk MJ; Pawlikowska L; DeYoung JA; Juijn JA; Liao M; Klomp LW; Lomri N; Berger R; Scharschmidt BF; Knisely AS; Houwen RH; Freimer NB Nat Genet; 1998 Mar; 18(3):219-24. PubMed ID: 9500542 [TBL] [Abstract][Full Text] [Related]
39. [Studies on the clinical manifestation and SLC25A13 gene mutation of Chinese patients with neonatal intrahepatic cholestasis caused by citrin deficiency]. Xing YZ; Qiu WJ; Ye J; Han LS; Xu SS; Zhang HW; Gao XL; Wang Y; Gu XF Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):180-5. PubMed ID: 20376801 [TBL] [Abstract][Full Text] [Related]
40. [The diagnosis of conjugated bilirubin jaundice in children]. Arion C; Popescu V Pediatrie (Bucur); 1990; 39(2):97-128. PubMed ID: 1966518 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]