| 000 | 01348 a2200361 4500 | ||
|---|---|---|---|
| 005 | 20250516081547.0 | ||
| 264 | 0 | _c20130509 | |
| 008 | 201305s 0 0 eng d | ||
| 022 | _a1708-8283 | ||
| 024 | 7 |
_a10.1177/0883073812437242 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGhosh, Partha S | |
| 245 | 0 | 0 |
_aPitt-Hopkins syndrome in a boy with Charcot Marie Tooth disease type 1A: a rare co-occurrence of 2 genetic disorders. _h[electronic resource] |
| 260 |
_bJournal of child neurology _cDec 2012 |
||
| 300 |
_a1602-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aBasic Helix-Loop-Helix Leucine Zipper Transcription Factors _xgenetics |
| 650 | 0 | 4 |
_aCharcot-Marie-Tooth Disease _xcomplications |
| 650 | 0 | 4 | _aElectroencephalography |
| 650 | 0 | 4 | _aFacies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHyperventilation _xcomplications |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIntellectual Disability _xcomplications |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aTranscription Factor 4 |
| 650 | 0 | 4 |
_aTranscription Factors _xgenetics |
| 700 | 1 | _aFriedman, Neil R | |
| 700 | 1 | _aGhosh, Debabrata | |
| 773 | 0 |
_tJournal of child neurology _gvol. 27 _gno. 12 _gp. 1602-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1177/0883073812437242 _zAvailable from publisher's website |
| 999 |
_c21586020 _d21586020 |
||