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The American Journal of Cardiology|September 25, 1999
Deletion 22q11 in patients with interrupted aortic archB Marino, M C Digilio, M Persiani, et al.Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.European Journal of Pediatrics|December 1, 1995
Noonan syndrome: structural abnormalities of the mitral valve causing subaortic obstructionB Marino, M G Gagliardi, M C Digilio, et al.American Journal of Medical Genetics|July 3, 1995
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8pF Amati, A Mari, R Mingarelli, et al.Italian Heart Journal : Official Journal of the Italian Federation of Cardiology|June 8, 2001
Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patternsS Anaclerio, B Marino, A Carotti, et al.Circulation|December 6, 2001
Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrenceM C Digilio, B Casey, A Toscano, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Anatomic patterns of conotruncal defects associated with deletion 22q11B Marino, M C Digilio, A Toscano, et al.Clinical Genetics|May 4, 2018
Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehogM C Digilio, F Pugnaloni, A De Luca, et al.Minerva Pediatrica|April 28, 2000
Langer-Giedion syndrome. A patient without mental retardation and a large 8q23.2-q24.22 deletionG Tiberio, M C Digilio, A GiannottiJournal of Insect Physiology|May 29, 2003
Host regulation effects of ovary fluid and venom of Aphidius ervi (Hymenoptera: Braconidae)E Tremblay, F Pennacchio, M C. DigilioPageof 34