| 000 | 01792 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250517113115.0 | ||
| 264 | 0 | _c20171101 | |
| 008 | 201711s 0 0 eng d | ||
| 022 | _a1468-6244 | ||
| 024 | 7 |
_a10.1136/jmedgenet-2016-104094 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aReuter, Miriam S | |
| 245 | 0 | 0 |
_aFOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _c01 2017 |
||
| 300 |
_a64-72 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aDevelopmental Disabilities _xgenetics |
| 650 | 0 | 4 |
_aForkhead Transcription Factors _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLanguage Disorders _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPoint Mutation _xgenetics |
| 650 | 0 | 4 |
_aSequence Deletion _xgenetics |
| 650 | 0 | 4 |
_aSpeech _xphysiology |
| 650 | 0 | 4 |
_aSpeech Disorders _xgenetics |
| 700 | 1 | _aRiess, Angelika | |
| 700 | 1 | _aMoog, Ute | |
| 700 | 1 | _aBriggs, Tracy A | |
| 700 | 1 | _aChandler, Kate E | |
| 700 | 1 | _aRauch, Anita | |
| 700 | 1 | _aStampfer, Miriam | |
| 700 | 1 | _aSteindl, Katharina | |
| 700 | 1 | _aGläser, Dieter | |
| 700 | 1 | _aJoset, Pascal | |
| 700 | 1 | _aKrumbiegel, Mandy | |
| 700 | 1 | _aRabe, Harald | |
| 700 | 1 | _aSchulte-Mattler, Uta | |
| 700 | 1 | _aBauer, Peter | |
| 700 | 1 | _aBeck-Wödl, Stefanie | |
| 700 | 1 | _aKohlhase, Jürgen | |
| 700 | 1 | _aReis, André | |
| 700 | 1 | _aZweier, Christiane | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 54 _gno. 1 _gp. 64-72 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmedgenet-2016-104094 _zAvailable from publisher's website |
| 999 |
_c26370213 _d26370213 |
||