1. Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case;Giancotti;Childs Nerv Syst,2014
2. Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome;Au;Prenat Diagn,2011
3. Postmortem computed tomography in a case of Apert Syndrome: correlation with conventional autopsy and prenatal ultrasound;Patel;Ultrasound Q,2010
4. Postnatal brain and skull growth in an Apert syndrome mouse model;Hill;Am J Med Genet A,2013
5. Three-dimensional ultrasound to detect Apert syndrome and improve patient understanding;Moes;S D Med,2011