| 000 | 01393 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250517074915.0 | ||
| 264 | 0 | _c20171220 | |
| 008 | 201712s 0 0 eng d | ||
| 022 | _a1708-8283 | ||
| 024 | 7 |
_a10.1177/0883073815627884 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKilic, Esra | |
| 245 | 0 | 0 |
_aA Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome. _h[electronic resource] |
| 260 |
_bJournal of child neurology _c06 2016 |
||
| 300 |
_a913-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 |
_aFace _xabnormalities |
| 650 | 0 | 4 | _aFacies |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 |
_aHirschsprung Disease _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xdiagnosis |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMicrocephaly _xdiagnosis |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aZinc Finger E-box Binding Homeobox 2 _xgenetics |
| 700 | 1 | _aCetinkaya, Arda | |
| 700 | 1 | _aUtine, Gülen Eda | |
| 700 | 1 | _aBoduroğlu, Koray | |
| 773 | 0 |
_tJournal of child neurology _gvol. 31 _gno. 7 _gp. 913-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1177/0883073815627884 _zAvailable from publisher's website |
| 999 |
_c25668279 _d25668279 |
||