TY  - GEN
AU  - Lim,Derek Hk
AU  - Maher,Eamonn R
TI  - Human imprinting syndromes
SN  - 1750-192X
PY  - 2012///0416
KW  - Adaptor Proteins, Signal Transducing
KW  - genetics
KW  - Angelman Syndrome
KW  - Beckwith-Wiedemann Syndrome
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 11
KW  - Chromosomes, Human, Pair 14
KW  - Chromosomes, Human, Pair 15
KW  - Chromosomes, Human, Pair 20
KW  - Chromosomes, Human, Pair 6
KW  - Diabetes Mellitus
KW  - Female
KW  - Fibrous Dysplasia, Polyostotic
KW  - Genomic Imprinting
KW  - physiology
KW  - Humans
KW  - Hydatidiform Mole
KW  - Multigene Family
KW  - Mutation
KW  - Prader-Willi Syndrome
KW  - Pregnancy
KW  - Pseudohypoparathyroidism
KW  - Silver-Russell Syndrome
KW  - Uniparental Disomy
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.2217/epi.09.24
ER  -