Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.

Source:http://linkedlifedata.com/resource/pubmed/id/20007505

Hum. Mol. Genet. 2010 Mar 1 19 5 803-14

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PMID
20007505