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