Digilio MC - Search Results

1

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.

Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C, Unolt M, Pelliccione E, Anaclerio S, Caprio C, Cioffi S, Bilio M, Baban A, Drago F, Digilio MC, Marino B, Baldini A. Mastromoro G, et al. Among authors: digilio mc. PLoS One. 2019 Apr 1;14(4):e0211170. doi: 10.1371/journal.pone.0211170. eCollection 2019. PLoS One. 2019. PMID: 30933971 Free PMC article.

2

Nonrandom association of atrioventricular canal and del (8p) syndrome.

Marino B, Reale A, Giannotti A, Digilio MC, Dallapiccola B. Marino B, et al. Among authors: digilio mc. Am J Med Genet. 1992 Feb 15;42(4):424-7. doi: 10.1002/ajmg.1320420404. Am J Med Genet. 1992. PMID: 1609823 Review.

3

[Trisomy 18 associated with atrioventricular canal].

Digilio MC, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. G Ital Cardiol. 1991 Apr;21(4):433-5. G Ital Cardiol. 1991. PMID: 1936748 Italian.

4

Atrioventricular canal associated with trisomy 9.

Marino B, Digilio MC, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: digilio mc. Chest. 1989 Dec;96(6):1420-1. doi: 10.1378/chest.96.6.1420. Chest. 1989. PMID: 2582851

5

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.

Amati F, Mari A, Digilio MC, Mingarelli R, Marino B, Giannotti A, Novelli G, Dallapiccola B. Amati F, et al. Among authors: digilio mc. Hum Genet. 1995 May;95(5):479-82. doi: 10.1007/BF00223856. Hum Genet. 1995. PMID: 7759065

6

Transposition of the great arteries associated with deletion of chromosome 22q11.

Melchionda S, Digilio MC, Mingarelli R, Novelli G, Scambler P, Marino B, Dallapiccola B. Melchionda S, et al. Among authors: digilio mc. Am J Cardiol. 1995 Jan 1;75(1):95-8. doi: 10.1016/s0002-9149(99)80541-4. Am J Cardiol. 1995. PMID: 7801879 No abstract available.

7

Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotype.

Digilio MC, Mingarelli R, Marino B, Giannotti A, Melchionda S, Dallapiccola B. Digilio MC, et al. Clin Genet. 1994 Sep;46(3):268-70. doi: 10.1111/j.1399-0004.1994.tb04240.x. Clin Genet. 1994. PMID: 7820944

8

Risk of congenital heart defects in relatives of patients with atrioventricular canal.

Digilio MC, Marino B, Cicini MP, Giannotti A, Formigari R, Dallapiccola B. Digilio MC, et al. Am J Dis Child. 1993 Dec;147(12):1295-7. doi: 10.1001/archpedi.1993.02160360037013. Am J Dis Child. 1993. PMID: 8249947

9

Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot.

Marino B, Digilio MC, Grazioli S, Formigari R, Mingarelli R, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: digilio mc. Am J Cardiol. 1996 Mar 1;77(7):505-8. doi: 10.1016/s0002-9149(97)89345-9. Am J Cardiol. 1996. PMID: 8629592

10

Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.

Digilio MC, Marino B, Grazioli S, Agostino D, Giannotti A, Dallapiccola B. Digilio MC, et al. Am J Cardiol. 1996 Jun 15;77(15):1375-6. doi: 10.1016/s0002-9149(96)00212-3. Am J Cardiol. 1996. PMID: 8677886

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