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42. UDPglucuronosyltransferase deficiency in man and animals. Roy Chowdhury J; Roy Chowdhury N; Arias IM Biochem Soc Trans; 1984 Feb; 12(1):81-3. PubMed ID: 6423423 [No Abstract] [Full Text] [Related]
44. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. Kadakol A; Ghosh SS; Sappal BS; Sharma G; Chowdhury JR; Chowdhury NR Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440 [TBL] [Abstract][Full Text] [Related]
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46. [Causes of hyperbilirubinemia in newborns and infants]. Iwańczak F; Prandota J; Iwańczak B Pediatr Pol; 1980 May; 55(5):61-8. PubMed ID: 6773020 [No Abstract] [Full Text] [Related]
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