Digilio MC - Search Results

1

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.

Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, Tran OT, Miller D, Lin JR, Zackai E, Johnston HR, Chow EWC, Vorstman JAS, Vingerhoets C, van Amelsvoort T, Gothelf D, Swillen A, Breckpot J, Vermeesch JR, Eliez S, Schneider M, van den Bree MBM, Owen MJ, Kates WR, Repetto GM, Shashi V, Schoch K, Bearden CE, Digilio MC, Unolt M, Putotto C, Marino B, Pontillo M, Armando M, Vicari S, Angkustsiri K, Campbell L, Busa T, Heine-Suñer D, Murphy KC, Murphy D, García-Miñaúr S, Fernández L; International 22q11.2 Brain and Behavior Consortium (IBBC); Zhang ZD, Goldmuntz E, Gur RE, Emanuel BS, Zheng D, Marshall CR, Bassett AS, Wang T, Morrow BE. Zhao Y, et al. Among authors: digilio mc. NPJ Genom Med. 2023 Jul 18;8(1):17. doi: 10.1038/s41525-023-00363-y. NPJ Genom Med. 2023. PMID: 37463940 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

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

4

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

5

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

6

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

7

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

8

Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canal.

Digilio MC, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. J Med Genet. 1996 May;33(5):416-8. doi: 10.1136/jmg.33.5.416. J Med Genet. 1996. PMID: 8733055 Free PMC article.

9

Chromosome 22q11 microdeletion and isolated conotruncal heart defects.

Digilio MC, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. Arch Dis Child. 1997 Jan;76(1):79-80. doi: 10.1136/adc.76.1.79a. Arch Dis Child. 1997. PMID: 9059172 Free PMC article. No abstract available.

10

Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.

Digilio MC, Marino B, Giannotti A, Toscano A, Dallapiccola B. Digilio MC, et al. J Med Genet. 1997 Mar;34(3):188-90. doi: 10.1136/jmg.34.3.188. J Med Genet. 1997. PMID: 9132487 Free PMC article.

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