Array-CGH and Clinical Characterization in a Patient With Subtelomeric 6p Deletion Without Ocular DysgenesisPICCIONE, Maria; ANTONA, R; SALZANO, E et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 150-154, issn 1552-4825, 5 p.Article

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

The First Case of Myoclonic Epilepsy in a Child With a De Novo 22q11.2 MicroduplicationPICCIONE, Maria; VECCHIO, Davide; CAVANI, Simona et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3054-3059, issn 1552-4825, 6 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

Clinical Significance of Rare Copy Number Variations in Epilepsy: A Case-Control Survey Using Microarray-Based Comparative Genomic HybridizationSTRIANO, Pasquale; COPPOLA, Antonietta; ELIA, Maurizio et al.Archives of neurology (Chicago). 2012, Vol 69, Num 3, pp 322-330, issn 0003-9942, 9 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

4q13.1-21.1 Deletion Encompassing the HPE8 Locus in an Adolescent With Intellectual Disability and Bilateral Microphthalmia, But Without HoloprosencephalyPICCIONE, Maria; SERRA, Gregorio; CONSIGLIO, Valeria et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 6, pp 1427-1433, issn 1552-4825, 7 p.Article

Phenotypic Analysis of Individuals With Costello Syndrome dye to HRAS p.G13CGRIPP, Karen W; HOPKINS, Elizabeth; GRAHAM, Gail E et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 4, pp 706-716, issn 1552-4825, 11 p.Article

A novel L1CAM mutation in a fetus detected by prenatal diagnosisPICCIONE, Maria; MATINA, Federico; FICHERA, Marco et al.European journal of pediatrics. 2010, Vol 169, Num 4, pp 415-419, issn 0340-6199, 5 p.Article

Bipolar disorders and affective temperaments : A national family study testing the endophenotype and subaffective theses using the TEMPS-A Buenos AiresVAZQUEZ, Gustavo H; KAHN, Clara; GARCIA BONETTO, Gerardo et al.Journal of affective disorders. 2008, Vol 108, Num 1-2, pp 25-32, issn 0165-0327, 8 p.Article