TY  - GEN
AU  - Reed,Robyn C
AU  - Kapur,Raj P
TI  - Hepatic mesenchymal hamartoma: a disorder of imprinting
SN  - 1093-5266
PY  - 2008///1028
KW  - Chromosome Aberrations
KW  - Genomic Imprinting
KW  - genetics
KW  - Hamartoma
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Liver Diseases
KW  - Loss of Heterozygosity
KW  - Mesoderm
KW  - pathology
KW  - Mutation
N1  - Publication Type: Comment; Journal Article
UR  - https://doi.org/10.2350/07-06-0291.1
ER  -