| 000 | 01622 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250517012418.0 | ||
| 264 | 0 | _c20160615 | |
| 008 | 201606s 0 0 eng d | ||
| 022 | _a1476-5438 | ||
| 024 | 7 |
_a10.1038/ejhg.2014.296 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSimpson, Nuala H | |
| 245 | 0 | 0 |
_aGenome-wide analysis identifies a role for common copy number variants in specific language impairment. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cOct 2015 |
||
| 300 |
_a1370-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 |
_aDNA Copy Number Variations _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aGenome _xgenetics |
| 650 | 0 | 4 |
_aGenome-Wide Association Study _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aLanguage |
| 650 | 0 | 4 |
_aLanguage Disorders _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
| 700 | 1 | _aCeroni, Fabiola | |
| 700 | 1 | _aReader, Rose H | |
| 700 | 1 | _aCovill, Laura E | |
| 700 | 1 | _aKnight, Julian C | |
| 700 | 1 | _aHennessy, Elizabeth R | |
| 700 | 1 | _aBolton, Patrick F | |
| 700 | 1 | _aConti-Ramsden, Gina | |
| 700 | 1 | _aO'Hare, Anne | |
| 700 | 1 | _aBaird, Gillian | |
| 700 | 1 | _aFisher, Simon E | |
| 700 | 1 | _aNewbury, Dianne F | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 23 _gno. 10 _gp. 1370-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ejhg.2014.296 _zAvailable from publisher's website |
| 999 |
_c24531028 _d24531028 |
||