000 | 01676 a2200469 4500 | ||
---|---|---|---|
005 | 20250516065252.0 | ||
264 | 0 | _c20120416 | |
008 | 201204s 0 0 eng d | ||
022 | _a1750-192X | ||
024 | 7 |
_a10.2217/epi.09.24 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aLim, Derek Hk | |
245 | 0 | 0 |
_aHuman imprinting syndromes. _h[electronic resource] |
260 |
_bEpigenomics _cDec 2009 |
||
300 |
_a347-69 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Review | ||
650 | 0 | 4 |
_aAdaptor Proteins, Signal Transducing _xgenetics |
650 | 0 | 4 |
_aAngelman Syndrome _xgenetics |
650 | 0 | 4 |
_aBeckwith-Wiedemann Syndrome _xgenetics |
650 | 0 | 4 |
_aChromosome Disorders _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 11 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 14 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 15 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 20 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 6 _xgenetics |
650 | 0 | 4 |
_aDiabetes Mellitus _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFibrous Dysplasia, Polyostotic _xgenetics |
650 | 0 | 4 |
_aGenomic Imprinting _xphysiology |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHydatidiform Mole _xgenetics |
650 | 0 | 4 |
_aMultigene Family _xgenetics |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 |
_aPrader-Willi Syndrome _xgenetics |
650 | 0 | 4 | _aPregnancy |
650 | 0 | 4 |
_aPseudohypoparathyroidism _xgenetics |
650 | 0 | 4 |
_aSilver-Russell Syndrome _xgenetics |
650 | 0 | 4 |
_aUniparental Disomy _xgenetics |
700 | 1 | _aMaher, Eamonn R | |
773 | 0 |
_tEpigenomics _gvol. 1 _gno. 2 _gp. 347-69 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.2217/epi.09.24 _zAvailable from publisher's website |
999 |
_c21348778 _d21348778 |