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 |