| 000 | 01618 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250515130810.0 | ||
| 264 | 0 | _c20081112 | |
| 008 | 200811s 0 0 eng d | ||
| 022 | _a1573-2665 | ||
| 024 | 7 |
_a10.1007/s10545-008-0877-y _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPotter, N L | |
| 245 | 0 | 0 |
_aCorrelates of language impairment in children with galactosaemia. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _cAug 2008 |
||
| 300 |
_a524-32 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aCognition _xphysiology |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGalactosemias _xcomplications |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant Nutritional Physiological Phenomena |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aLanguage Development Disorders _xetiology |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMilk _xphysiology |
| 650 | 0 | 4 | _aParents |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aRisk Factors |
| 650 | 0 | 4 | _aSocioeconomic Factors |
| 650 | 0 | 4 | _aSpeech Therapy |
| 650 | 0 | 4 |
_aUTP-Hexose-1-Phosphate Uridylyltransferase _xgenetics |
| 700 | 1 | _aLazarus, J-A C | |
| 700 | 1 | _aJohnson, J M | |
| 700 | 1 | _aSteiner, R D | |
| 700 | 1 | _aShriberg, L D | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 31 _gno. 4 _gp. 524-32 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10545-008-0877-y _zAvailable from publisher's website |
| 999 |
_c18128648 _d18128648 |
||