| 000 | 01835 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250516074719.0 | ||
| 264 | 0 | _c20120327 | |
| 008 | 201203s 0 0 eng d | ||
| 022 | _a1098-4275 | ||
| 024 | 7 |
_a10.1542/peds.2011-0739 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aO'Callaghan, Michael E | |
| 245 | 0 | 0 |
_aFetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study. _h[electronic resource] |
| 260 |
_bPediatrics _cFeb 2012 |
||
| 300 |
_ae414-23 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aApolipoproteins E _xgenetics |
| 650 | 0 | 4 | _aAustralia |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 |
_aCerebral Palsy _xepidemiology |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aGenetic Carrier Screening |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aHaplotypes _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aMannose-Binding Lectin _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aProthrombin _xgenetics |
| 700 | 1 | _aMaclennan, Alastair H | |
| 700 | 1 | _aGibson, Catherine S | |
| 700 | 1 | _aMcMichael, Gai L | |
| 700 | 1 | _aHaan, Eric A | |
| 700 | 1 | _aBroadbent, Jessica L | |
| 700 | 1 | _aGoldwater, Paul N | |
| 700 | 1 | _aPainter, Jodie N | |
| 700 | 1 | _aMontgomery, Grant W | |
| 700 | 1 | _aDekker, Gus A | |
| 773 | 0 |
_tPediatrics _gvol. 129 _gno. 2 _gp. e414-23 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1542/peds.2011-0739 _zAvailable from publisher's website |
| 999 |
_c21504344 _d21504344 |
||