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Archives of Virology. Supplementum|January 1, 1992
Effect of prednisone priming followed by alfa-interferon in treatment of children with chronic hepatitis B: an interim analysis of a controlled trialR Utili, E Sagnelli, G Giusti, 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.
American Journal of Human Genetics|December 27, 2011
Deletion of KDM6A, a histone demethylase interacting with MLL2, in three patients with Kabuki syndromeDamien Lederer, Bernard Grisart, Maria Cristina Digilio, et al.
Clinical Dysmorphology|March 15, 2006
Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of FallotPasquale Vergara, Maria Cristina Digilio, Andrea De Zorzi, et al.
American Journal of Medical Genetics. Part A|January 26, 2005
Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2M Cristina Digilio, Bruno Marino, Rossella Capolino, et al.
Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2014
Behavioral phenotype in Costello syndrome with atypical mutation: a case reportPaolo Alfieri, Cristina Caciolo, Giorgia Piccini, et al.
Frontiers in Physiology|July 24, 2019
Trichoderma atroviride P1 Colonization of Tomato Plants Enhances Both Direct and Indirect Defense Barriers Against InsectsMariangela Coppola, Pasquale Cascone, Ilaria Di Lelio, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 3, 2004
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutationsM Cristina Digilio, Giuseppe Pacileo, Anna Sarkozy, et al.
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