A. Battaglia

The inv dup(15) syndrome

A. Battaglia, E. Bertini, G. Neri, 1997, Neurology.

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

A. Battaglia, R. Tenconi, G. Neri, 2000, American journal of medical genetics.

Erratum: Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation( Pediatrics (2008) 121 (404-410))

C. Romano, E. Zackai, H. Hoyme, 2008 .

Case of apparent Gurrieri syndrome showing molecular findings of Angelman syndrome.

F. Gurrieri, A. Battaglia, 1999, American journal of medical genetics.

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

G. Scarano, G. Neri, M. Cappa, 1994, American journal of medical genetics.

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13

R. Tancredi, F. Gurrieri, E. Sangiorgi, 1999, Neurology.

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.

M. Altherr, M. Zollino, C. Di Stefano, 1999, American journal of medical genetics.