| 000 | 01709 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250515014611.0 | ||
| 264 | 0 | _c20060530 | |
| 008 | 200605s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.31110 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZeesman, Susan | |
| 245 | 0 | 0 |
_aSpeech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cMar 2006 |
||
| 300 |
_a509-14 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 |
_aApraxias _xpathology |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Banding |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 7 _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aForkhead Transcription Factors _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 |
_aLanguage Disorders _xpathology |
| 650 | 0 | 4 |
_aMicrosatellite Repeats _xgenetics |
| 650 | 0 | 4 |
_aSpeech Disorders _xpathology |
| 700 | 1 | _aNowaczyk, Małgorzata J M | |
| 700 | 1 | _aTeshima, Ikuko | |
| 700 | 1 | _aRoberts, Wendy | |
| 700 | 1 | _aCardy, Janis Oram | |
| 700 | 1 | _aBrian, Jessica | |
| 700 | 1 | _aSenman, Lili | |
| 700 | 1 | _aFeuk, Lars | |
| 700 | 1 | _aOsborne, Lucy R | |
| 700 | 1 | _aScherer, Stephen W | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 140 _gno. 5 _gp. 509-14 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.31110 _zAvailable from publisher's website |
| 999 |
_c16083371 _d16083371 |
||