Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome.

Source:http://linkedlifedata.com/resource/pubmed/id/18074389

Am. J. Med. Genet. A 2008 Jan 1 146A 1 103-9

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18074389