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Clinical and Experimental Immunology|July 11, 2000
T cell receptor repertoire and function in patients with DiGeorge syndrome and velocardiofacial syndromeM Pierdominici, M Marziali, A Giovannetti, et al.Molecular Syndromology|December 23, 2011
RASopathies: Clinical Diagnosis in the First Year of LifeM C Digilio, F Lepri, A Baban, et al.Clinical and Experimental Immunology|April 18, 2003
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)M Pierdominici, F Mazzetta, E Caprini, et al.Journal of Medical Genetics|January 1, 1995
An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE)A Giannotti, M C Digilio, R Mingarelli, et al.Clinical Genetics|September 3, 2010
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricleAlessandro De Luca, A Sarkozy, R Ferese, et al.European Journal of Medical Genetics|November 11, 2021
Congenital heart defects in the recurrent 2q13 deletion syndromeM C Digilio, M L Dentici, S Loddo, et al.Clinical Genetics|December 6, 2012
Syndromic non-compaction of the left ventricle: associated chromosomal anomaliesM C Digilio, L Bernardini, M G Gagliardi, et al.Pediatric Surgery International|June 20, 2007
Congenital diaphragmatic hernia in CHARGE syndromeG Casaccia, M C Digilio, P L Seymandi, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1993
Congenital heart disease in patients with Down's syndrome: anatomic and genetic aspectsB MarinoPageof 34