| 000 | 01416 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250516020435.0 | ||
| 264 | 0 | _c20110531 | |
| 008 | 201105s 0 0 eng d | ||
| 022 | _a1476-5438 | ||
| 024 | 7 |
_a10.1038/ejhg.2010.218 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBaple, Emma L | |
| 245 | 0 | 0 |
_aAn atypical case of hypomethylation at multiple imprinted loci. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cMar 2011 |
||
| 300 |
_a360-2 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAngelman Syndrome _xgenetics |
| 650 | 0 | 4 |
_aBeckwith-Wiedemann Syndrome _xgenetics |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aDNA Methylation |
| 650 | 0 | 4 | _aEpigenomics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Loci |
| 650 | 0 | 4 | _aGenomic Imprinting |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMultigene Family |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPrader-Willi Syndrome _xgenetics |
| 700 | 1 | _aPoole, Rebecca L | |
| 700 | 1 | _aMansour, Sahar | |
| 700 | 1 | _aWilloughby, Catherine | |
| 700 | 1 | _aTemple, I Karen | |
| 700 | 1 | _aDocherty, Louise E | |
| 700 | 1 | _aTaylor, Rohan | |
| 700 | 1 | _aMackay, Deborah J G | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 19 _gno. 3 _gp. 360-2 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ejhg.2010.218 _zAvailable from publisher's website |
| 999 |
_c20492142 _d20492142 |
||