TY  - GEN
AU  - Eggermann,Thomas
AU  - Elbracht,Miriam
AU  - Schröder,Carmen
AU  - Reutter,Heiko
AU  - Soellner,Lukas
AU  - Spengler,Sabrina
AU  - Begemann,Matthias
TI  - Congenital imprinting disorders: a novel mechanism linking seemingly unrelated disorders
SN  - 1097-6833
PY  - 2013///1205
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Mapping
KW  - DNA Methylation
KW  - Epigenesis, Genetic
KW  - Female
KW  - Genetic Association Studies
KW  - Genomic Imprinting
KW  - Heterozygote
KW  - Humans
KW  - Infant
KW  - Male
KW  - Phenotype
KW  - Syndrome
KW  - Uniparental Disomy
N1  - Publication Type: Clinical Conference; Journal Article
UR  - https://doi.org/10.1016/j.jpeds.2013.05.017
ER  -