Found: 3
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Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
- Published in:
- Journal of Human Genetics, 1999, v. 44, n. 1, p. 22, doi. 10.1007/s100380050100
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- Publication type:
- Article
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: The common−3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.
- Published in:
- Pediatrics International, 2005, v. 47, n. 2, p. 137, doi. 10.1111/j.1442-200x.2005.02030.x
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- Publication type:
- Article
Mutation analysis of phenylketonuria in Yamagata prefecture, Japan.
- Published in:
- Pediatrics International, 2001, v. 43, n. 1, p. 1, doi. 10.1046/j.1442-200X.2001.01336.x
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- Publication type:
- Article