000 01367 a2200421 4500
005 20250517102213.0
264 0 _c20170209
008 201702s 0 0 eng d
022 _a1676-5680
024 7 _a10.4238/gmr.15028373
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGuo, X H
245 0 0 _aAnalysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia.
_h[electronic resource]
260 _bGenetics and molecular research : GMR
_cMay 2016
500 _aPublication Type: Journal Article
650 0 4 _aBilirubin
_xblood
650 0 4 _aFemale
650 0 4 _aGene Frequency
650 0 4 _aGenetic Association Studies
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenotype
650 0 4 _aGlucuronosyltransferase
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aHyperbilirubinemia, Hereditary
_xblood
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPolymorphism, Single Nucleotide
700 1 _aSun, Y F
700 1 _aCui, M
700 1 _aWang, J B
700 1 _aHan, S Z
700 1 _aMiao, J
773 0 _tGenetics and molecular research : GMR
_gvol. 15
_gno. 2
856 4 0 _uhttps://doi.org/10.4238/gmr.15028373
_zAvailable from publisher's website
999 _c26142909
_d26142909