Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndromePICCIONE, Maria; ANTONA, Vincenzo; NICETA, Marcello et al.European journal of pediatrics. 2009, Vol 168, Num 9, pp 1135-1139, issn 0340-6199, 5 p.Article

10qter Deletion : A New CasePICCIONE, Maria; ANTONA, Vincenzo; PIRO, Ettore et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 18, pp 2435-2438, issn 1552-4825, 4 p.Article

Array CGH defined interstitial deletion on chromosome 14: a new casePICCIONE, Maria; ANTONA, Vincenzo; SCAVONE, Valeria et al.European journal of pediatrics. 2010, Vol 169, Num 7, pp 845-851, issn 0340-6199, 7 p.Article

Array-CGH Defined Chromosome 1p Duplication in a patient With Autism Spectrum Disorder, Mild Mental Deficiency, and Minor Dysmorphic FeaturesPICCIONE, Maria; ANTONA, Vincenzo; ANTONA, Roberta et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 2, pp 486-489, issn 1552-4825, 4 p.Article