TY  - GEN
AU  - Müller,Anne
AU  - Soellner,Lukas
AU  - Binder,Gerhard
AU  - Begemann,Matthias
AU  - Eggermann,Thomas
TI  - No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders
SN  - 1552-4833
PY  - 2016///1019
KW  - Beckwith-Wiedemann Syndrome
KW  - genetics
KW  - Chromosomes, Human, Pair 11
KW  - Fetal Growth Retardation
KW  - Genetic Testing
KW  - Genomic Imprinting
KW  - Humans
KW  - Insulin-Like Growth Factor II
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.37416
ER  -