TY  - GEN
AU  - Eggermann,Thomas
AU  - Binder,Gerhard
AU  - Brioude,Frédéric
AU  - Maher,Eamonn R
AU  - Lapunzina,Pablo
AU  - Cubellis,Maria Vittoria
AU  - Bergadá,Ignacio
AU  - Prawitt,Dirk
AU  - Begemann,Matthias
TI  - CDKN1C mutations: two sides of the same coin
SN  - 1471-499X
PY  - 2015///0723
KW  - Adrenal Insufficiency
KW  - diagnosis
KW  - Animals
KW  - Beckwith-Wiedemann Syndrome
KW  - Chromosome Aberrations
KW  - Chromosomes, Human, Pair 11
KW  - Cyclin-Dependent Kinase Inhibitor p57
KW  - genetics
KW  - Disease Management
KW  - Fetal Growth Retardation
KW  - Genetic Association Studies
KW  - Genetic Counseling
KW  - Genomic Imprinting
KW  - Humans
KW  - Mutation
KW  - Osteochondrodysplasias
KW  - Urogenital Abnormalities
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1016/j.molmed.2014.09.001
ER  -