000 01488 a2200469 4500
005 20250516155610.0
264 0 _c20131205
008 201312s 0 0 eng d
022 _a1097-6833
024 7 _a10.1016/j.jpeds.2013.05.017
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aEggermann, Thomas
245 0 0 _aCongenital imprinting disorders: a novel mechanism linking seemingly unrelated disorders.
_h[electronic resource]
260 _bThe Journal of pediatrics
_cOct 2013
300 _a1202-7 p.
_bdigital
500 _aPublication Type: Clinical Conference; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Mapping
650 0 4 _aDNA Methylation
650 0 4 _aEpigenesis, Genetic
650 0 4 _aFemale
650 0 4 _aGenetic Association Studies
650 0 4 _aGenomic Imprinting
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aSyndrome
650 0 4 _aUniparental Disomy
_xgenetics
700 1 _aElbracht, Miriam
700 1 _aSchröder, Carmen
700 1 _aReutter, Heiko
700 1 _aSoellner, Lukas
700 1 _aSpengler, Sabrina
700 1 _aBegemann, Matthias
773 0 _tThe Journal of pediatrics
_gvol. 163
_gno. 4
_gp. 1202-7
856 4 0 _uhttps://doi.org/10.1016/j.jpeds.2013.05.017
_zAvailable from publisher's website
999 _c22874627
_d22874627