CajaibaMMSarita-ReyesCZambranoEReyes-MugicaM. Mesenchymal hamartoma of the liver associated with Beckwith-Weidemann syndrome features and high serum-alphafetoprotein levels. Pediatr Dev Pathol2007;10:233–238.
2.
RakhejaDMargrafLRRomlinsonGESchneiderNR. Hepatic mesenchymal hamartoma with translocation involving chromosome band 19q13.4: a recurrent abnormality. Cancer Genet Cytogenet2004;153:60–63.
3.
YooS-HParkHJChoSYKimCJ. Mesenchymal hamartoma of the liver in Beckwith-Wiedemann syndrome: a case report. Korean J Pathol2002;36:425–428.
4.
Garcia-de-la-TorreJPSotelo-RodriguezMTSantos-BrizARodriguez-PeraltoJL. Mesenchymal hamartoma of the liver in Beckwith-Wiedemann syndrome: the first reported case. Pediatr Pathol Mol Med2000;19:455–460.
5.
FrancisBHallamLKecskesZEllwoodDCroakerDKentA. Placental mesenchymal dysplasia associated with hepatic mesenchymal hamartoma in the newborn. Pediatr Dev Pathol2007;10:50–54.
6.
AlwaidhMHWoodhallCRCartyHT. Mesenchymal hamartoma of the liver: a case report. Pediatr Radiol1997;17:247–249.
7.
KitanoYRuchelliEWeinerSAdzickNS. Hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta. Fetal Diagn Ther2000;15:134–138.
8.
LabergeJ-MPatenaudeYDesiletsV. Large hepatic mesenchymal hamartoma leading to mid-trimester fetal demise. Fetal Diagn Ther2005;20:141–145.
9.
CartaMMaresiEGiuffreM. Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: a case report. J Pediatr Surg2005;40:E37–E39.
10.
TalmonGACohenSM. Mesenchymal hamartoma of the liver with an interstitial deletion involving chromosome band 19q13.4: a theory as to pathogenesis?Arch Pathol Lab Med2006;130:1216–1218.
11.
BaboiuO-ESaalHCollinsM. Hepatic mesenchymal hamartoma: cytogenetic analysis of a case and review of the literature. Pediatr Dev Pathol2008;11:295–299.
12.
Kaiser-RogersKAMcFaddenDELivasyCA. Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia. J Med Genet2006;43:187–192.
13.
SmithACChoufaniSFerreiraJCWeksbergR. Growth regulation, imprinted genes, and chromosome 11p15.5. Pediatr Res2007;61:43R–47R.
14.
KohdaTAsaiAKuroiwaY. Tumour suppressor activity of human imprinted gene PEG3 in a glioma cell line. Genes Cells2001;6:237–247.
