000 01371 a2200409 4500
005 20250513191041.0
264 0 _c19990924
008 199909s 0 0 eng d
022 _a1359-2998
024 7 _a10.1136/fn.81.2.f144
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMaier, R F
245 0 0 _aHFE gene mutation and transferrin saturation in very low birthweight infants.
_h[electronic resource]
260 _bArchives of disease in childhood. Fetal and neonatal edition
_cSep 1999
300 _aF144-5 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHLA Antigens
_xgenetics
650 0 4 _aHemochromatosis Protein
650 0 4 _aHistocompatibility Antigens Class I
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aInfant, Very Low Birth Weight
_xblood
650 0 4 _aMale
650 0 4 _aMembrane Proteins
650 0 4 _aMutation
650 0 4 _aProspective Studies
650 0 4 _aRetrospective Studies
650 0 4 _aTransferrin
_xmetabolism
700 1 _aWitt, H
700 1 _aBührer, C
700 1 _aMönch, E
700 1 _aKöttgen, E
773 0 _tArchives of disease in childhood. Fetal and neonatal edition
_gvol. 81
_gno. 2
_gp. F144-5
856 4 0 _uhttps://doi.org/10.1136/fn.81.2.f144
_zAvailable from publisher's website
999 _c10405907
_d10405907