Giannotti A - Search Results

1

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: giannotti a. Am J Cardiol. 1996 Mar 1;77(7):505-8. doi: 10.1016/s0002-9149(97)89345-9. Am J Cardiol. 1996. PMID: 8629592

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: giannotti a. 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

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: giannotti a. Hum Genet. 1995 May;95(5):479-82. doi: 10.1007/BF00223856. Hum Genet. 1995. PMID: 7759065

4

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. Among authors: giannotti a. Am J Cardiol. 1996 Jun 15;77(15):1375-6. doi: 10.1016/s0002-9149(96)00212-3. Am J Cardiol. 1996. PMID: 8677886

5

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. Among authors: giannotti a. 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.

6

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. Among authors: giannotti a. 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.

7

Tricuspid atresia and 22q11 deletion.

Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: giannotti a. Am J Med Genet. 1997 Oct 3;72(1):40-2. doi: 10.1002/(sici)1096-8628(19971003)72:1<40::aid-ajmg8>3.0.co;2-z. Am J Med Genet. 1997. PMID: 9295072

8

Deletion 22q11 in patients with interrupted aortic arch.

Marino B, Digilio MC, Persiani M, Di Donato R, Toscano A, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: giannotti a. Am J Cardiol. 1999 Aug 1;84(3):360-1, A9. doi: 10.1016/s0002-9149(99)00297-0. Am J Cardiol. 1999. PMID: 10496456

9

Anatomic patterns of conotruncal defects associated with deletion 22q11.

Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B. Marino B, et al. Among authors: giannotti a. Genet Med. 2001 Jan-Feb;3(1):45-8. doi: 10.1097/00125817-200101000-00010. Genet Med. 2001. PMID: 11339377 Free article.

10

Congenital heart defects in Kabuki syndrome.

Digilio MC, Marino B, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am J Med Genet. 2001 May 15;100(4):269-74. doi: 10.1002/ajmg.1265. Am J Med Genet. 2001. PMID: 11343317 Review.

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