| 000 | 01846 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250515225212.0 | ||
| 264 | 0 | _c20110519 | |
| 008 | 201105s 0 0 eng d | ||
| 022 | _a1476-4954 | ||
| 024 | 7 |
_a10.3109/14767058.2010.490889 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNarter, Fatma | |
| 245 | 0 | 0 |
_aNeonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients. _h[electronic resource] |
| 260 |
_bThe journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians _cFeb 2011 |
||
| 300 |
_a313-6 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aArginine _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aGestational Age |
| 650 | 0 | 4 |
_aGlucuronosyltransferase _xgenetics |
| 650 | 0 | 4 |
_aGlycine _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHyperbilirubinemia, Neonatal _xgenetics |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aTurkey |
| 700 | 1 | _aCan, Gülay | |
| 700 | 1 | _aErgen, Arzu | |
| 700 | 1 | _aIsbir, Turgay | |
| 700 | 1 | _aInce, Zeynep | |
| 700 | 1 | _aÇoban, Asuman | |
| 773 | 0 |
_tThe journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians _gvol. 24 _gno. 2 _gp. 313-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.3109/14767058.2010.490889 _zAvailable from publisher's website |
| 999 |
_c19878643 _d19878643 |
||