000 01478 a2200397 4500
005 20250516073306.0
264 0 _c20120720
008 201207s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.34412
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBegemann, Matthias
245 0 0 _aSegmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylation.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cFeb 2012
300 _a423-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCalcium-Binding Proteins
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 14
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aDNA Methylation
_xgenetics
650 0 4 _aHumans
650 0 4 _aIntercellular Signaling Peptides and Proteins
_xgenetics
650 0 4 _aMale
650 0 4 _aMembrane Proteins
_xgenetics
650 0 4 _aProteins
_xgenetics
650 0 4 _aRNA, Long Noncoding
650 0 4 _aSilver-Russell Syndrome
_xdiagnosis
650 0 4 _aUniparental Disomy
_xdiagnosis
700 1 _aSpengler, Sabrina
700 1 _aKordass, Ulrike
700 1 _aSchröder, Carmen
700 1 _aEggermann, Thomas
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 158A
_gno. 2
_gp. 423-8
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.34412
_zAvailable from publisher's website
999 _c21462505
_d21462505