000 01247 a2200325 4500
005 20250517055150.0
264 0 _c20161019
008 201610s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.37416
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMüller, Anne
245 0 0 _aNo major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJan 2016
300 _a283-4 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't
650 0 4 _aBeckwith-Wiedemann Syndrome
_xgenetics
650 0 4 _aChromosomes, Human, Pair 11
_xgenetics
650 0 4 _aFetal Growth Retardation
_xgenetics
650 0 4 _aGenetic Testing
650 0 4 _aGenomic Imprinting
_xgenetics
650 0 4 _aHumans
650 0 4 _aInsulin-Like Growth Factor II
_xgenetics
700 1 _aSoellner, Lukas
700 1 _aBinder, Gerhard
700 1 _aBegemann, Matthias
700 1 _aEggermann, Thomas
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 170A
_gno. 1
_gp. 283-4
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.37416
_zAvailable from publisher's website
999 _c25334843
_d25334843