| 000 | 01590 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250515054708.0 | ||
| 264 | 0 | _c20070222 | |
| 008 | 200702s 0 0 eng d | ||
| 022 | _a1531-5037 | ||
| 024 | 7 |
_a10.1016/j.jpedsurg.2006.10.022 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aOu-Yang, Mei-Chen | |
| 245 | 0 | 0 |
_aConcomitant existence of total bowel aganglionosis and congenital central hypoventilation syndrome in a neonate with PHOX2B gene mutation. _h[electronic resource] |
| 260 |
_bJournal of pediatric surgery _cFeb 2007 |
||
| 300 |
_ae9-11 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aDisease Progression |
| 650 | 0 | 4 | _aFatal Outcome |
| 650 | 0 | 4 |
_aHirschsprung Disease _xcomplications |
| 650 | 0 | 4 |
_aHomeodomain Proteins _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypoventilation _xcomplications |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMultiple Organ Failure _xdiagnosis |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aRare Diseases |
| 650 | 0 | 4 | _aRisk Assessment |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 |
_aTranscription Factors _xgenetics |
| 700 | 1 | _aYang, San-Nan | |
| 700 | 1 | _aHsu, Yung-Ming | |
| 700 | 1 | _aOu-Yang, Mei-Hui | |
| 700 | 1 | _aHaung, Hsin-Chun | |
| 700 | 1 | _aLee, Shin-Yi | |
| 700 | 1 | _aHsieh, Wu-Shiun | |
| 700 | 1 | _aSu, Yi-Ning | |
| 700 | 1 | _aLiu, Chieh-An | |
| 773 | 0 |
_tJournal of pediatric surgery _gvol. 42 _gno. 2 _gp. e9-11 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.jpedsurg.2006.10.022 _zAvailable from publisher's website |
| 999 |
_c16831460 _d16831460 |
||