| 000 | 01320 a2200349 4500 | ||
|---|---|---|---|
| 005 | 20250516105735.0 | ||
| 264 | 0 | _c20130904 | |
| 008 | 201309s 0 0 eng d | ||
| 022 | _a1476-5438 | ||
| 024 | 7 |
_a10.1038/ejhg.2012.166 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNewbury, Dianne F | |
| 245 | 0 | 0 |
_aDual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cApr 2013 |
||
| 300 |
_a361-5 p. _bdigital |
||
| 500 | _aPublication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Comment | ||
| 650 | 0 | 4 |
_aApraxias _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 16 _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aSequence Deletion |
| 700 | 1 | _aMari, Francesca | |
| 700 | 1 | _aSadighi Akha, Elham | |
| 700 | 1 | _aMacdermot, Kay D | |
| 700 | 1 | _aCanitano, Roberto | |
| 700 | 1 | _aMonaco, Anthony P | |
| 700 | 1 | _aTaylor, Jenny C | |
| 700 | 1 | _aRenieri, Alessandra | |
| 700 | 1 | _aFisher, Simon E | |
| 700 | 1 | _aKnight, Samantha J L | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 21 _gno. 4 _gp. 361-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ejhg.2012.166 _zAvailable from publisher's website |
| 999 |
_c22040566 _d22040566 |
||