| 000 | 01802 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250514163908.0 | ||
| 264 | 0 | _c20040115 | |
| 008 | 200401s 0 0 eng d | ||
| 022 | _a0021-972X | ||
| 024 | 7 |
_a10.1210/jc.2003-031080 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aOwen, Catherine J | |
| 245 | 0 | 0 |
_aMutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome. _h[electronic resource] |
| 260 |
_bThe Journal of clinical endocrinology and metabolism _cDec 2003 |
||
| 300 |
_a6034-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aBase Sequence _xgenetics |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 |
_aDNA _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDNA-Binding Proteins _xgenetics |
| 650 | 0 | 4 | _aDosage Compensation, Genetic |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aForkhead Transcription Factors |
| 650 | 0 | 4 | _aGenetic Heterogeneity |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aImmune System Diseases _xgenetics |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntestinal Diseases _xgenetics |
| 650 | 0 | 4 | _aLod Score |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPolyendocrinopathies, Autoimmune _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aJennings, Claire E | |
| 700 | 1 | _aImrie, Helen | |
| 700 | 1 | _aLachaux, Alain | |
| 700 | 1 | _aBridges, Nicola A | |
| 700 | 1 | _aCheetham, Tim D | |
| 700 | 1 | _aPearce, Simon H S | |
| 773 | 0 |
_tThe Journal of clinical endocrinology and metabolism _gvol. 88 _gno. 12 _gp. 6034-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1210/jc.2003-031080 _zAvailable from publisher's website |
| 999 |
_c14403859 _d14403859 |
||