TY  - GEN
AU  - Baple,Emma L
AU  - Poole,Rebecca L
AU  - Mansour,Sahar
AU  - Willoughby,Catherine
AU  - Temple,I Karen
AU  - Docherty,Louise E
AU  - Taylor,Rohan
AU  - Mackay,Deborah J G
TI  - An atypical case of hypomethylation at multiple imprinted loci
SN  - 1476-5438
PY  - 2011///0531
KW  - Angelman Syndrome
KW  - genetics
KW  - Beckwith-Wiedemann Syndrome
KW  - Child, Preschool
KW  - DNA Methylation
KW  - Epigenomics
KW  - Female
KW  - Genetic Loci
KW  - Genomic Imprinting
KW  - Humans
KW  - Multigene Family
KW  - Mutation
KW  - Prader-Willi Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ejhg.2010.218
ER  -