000 01321 a2200313 4500
005 20250514022509.0
264 0 _c20020213
008 200202s 0 0 eng d
022 _a0743-8346
024 7 _a10.1038/sj.jp.7210630
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKaplan, M
245 0 0 _aGenetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
_h[electronic resource]
260 _bJournal of perinatology : official journal of the California Perinatal Association
_cDec 2001
300 _aS30-4; discussion S35-9 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aBilirubin
_xmetabolism
650 0 4 _aGilbert Disease
_xcomplications
650 0 4 _aGlucuronosyltransferase
_xmetabolism
650 0 4 _aGlycogen Storage Disease Type I
_xcomplications
650 0 4 _aHemolysis
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aJaundice, Neonatal
_xetiology
650 0 4 _aLiver
_xmetabolism
650 0 4 _aPromoter Regions, Genetic
773 0 _tJournal of perinatology : official journal of the California Perinatal Association
_gvol. 21 Suppl 1
_gp. S30-4; discussion S35-9
856 4 0 _uhttps://doi.org/10.1038/sj.jp.7210630
_zAvailable from publisher's website
999 _c11714204
_d11714204