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

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

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

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome : Five new casesSTRIANO, Pasquale; MALACARNE, Michela; GAGGERO, Roberto et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 18, pp 1944-1949, issn 1552-4825, 6 p.Article

The Refinement of the Critical Region for the 2q31.2q32.3 Deletion Syndrome Indicates Candidate Genes for Mental Retardation and Speech ImpairmentCOCCHELLA, Alessandro; MALACARNE, Michela; FORZANO, Francesca et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 7, pp 1342-1346, issn 1552-4841, 5 p.Article

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern : A report of five casesELIA, Maurizio; STRIANO, Pasquale; ROMANO, Corrado et al.Epilepsia (Copenhagen). 2006, Vol 47, Num 5, pp 830-838, issn 0013-9580, 9 p.Article

The natural history of Cri du Chat Syndrome. A report from the Italian RegisterMAINARDI, Paola Cerruti; PASTORE, Guido; CASTRONOVO, Chiara et al.European journal of medical genetics. 2006, Vol 49, Num 5, pp 363-383, issn 1769-7212, 21 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

Phenotype resembling donnai-barrow syndrome in a patient with 9qter;16qter unbalanced translocationFERRERO, Giovanni Battista; BELLIGNI, Elga; SORASIO, Lorena et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 8, pp 892-894, issn 1552-4825, 3 p.Article

FMR1, FMR2, and SLITRK2 Deletion Inside a Paracentric Inversion Involving Bands Xq27.3―q28 in a Male and His MotherCAVANI, Simona; PRONTERA, Paolo; GRASSO, Marina et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 1, pp 221-224, issn 1552-4825, 4 p.Article

A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5qMONICA, Matteo Della; LONARDO, Fortunato; FARAVELLI, Francesca et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 22, pp 2733-2737, issn 1552-4825, 5 p.Article

Mild generalized epilepsy and developmental disorder associated with large inv dup(15)CHIFARI, Rosanna; GUERRINI, Renzo; PIERLUIGI, Mauro et al.Epilepsia (Copenhagen). 2002, Vol 43, Num 9, pp 1096-1100, issn 0013-9580Article