Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.

Source:http://linkedlifedata.com/resource/pubmed/id/18245780

Hum. Mol. Genet. 2008 May 15 17 10 1427-35

Download in:

View as

Triples

General Info

PMID
18245780