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.

American journal of medical genetics. Part A

2008

https://researcherprofiles.org/profile/539029917

18074389

So J, Müller I, Kunath M, Herrmann S, Ullmann R, Schweiger S