| 000 | 01407 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250515085920.0 | ||
| 264 | 0 | _c20101029 | |
| 008 | 201010s 0 0 chi d | ||
| 022 | _a0578-1310 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGong, Chun-xiu | |
| 245 | 0 | 0 |
_a[Allgrove syndrome in the mainland of China: clinical report and mutation analysis]. _h[electronic resource] |
| 260 |
_bZhonghua er ke za zhi = Chinese journal of pediatrics _cJun 2007 |
||
| 300 |
_a422-5 p. _bdigital |
||
| 500 | _aPublication Type: English Abstract; Journal Article | ||
| 650 | 0 | 4 |
_aAdrenal Insufficiency _xgenetics |
| 650 | 0 | 4 |
_aAdrenocorticotropic Hormone _xblood |
| 650 | 0 | 4 | _aChina |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 |
_aDNA _xanalysis |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aEsophageal Achalasia _xgenetics |
| 650 | 0 | 4 | _aExons |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLacrimal Apparatus Diseases _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNerve Tissue Proteins _xgenetics |
| 650 | 0 | 4 |
_aNuclear Pore Complex Proteins _xgenetics |
| 650 | 0 | 4 |
_aOptic Atrophy _xgenetics |
| 700 | 1 | _aWen, Ya-ran | |
| 700 | 1 | _aZhao, Xiu-li | |
| 700 | 1 | _aSu, Chang | |
| 700 | 1 | _aCao, Bing-yan | |
| 700 | 1 | _aZhang, Xue | |
| 773 | 0 |
_tZhonghua er ke za zhi = Chinese journal of pediatrics _gvol. 45 _gno. 6 _gp. 422-5 |
|
| 999 |
_c17405378 _d17405378 |
||