Marino B - Search Results

1

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

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

2

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2.

Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet A. 2005 Apr 15;134A(2):158-64. doi: 10.1002/ajmg.a.30587. Am J Med Genet A. 2005. PMID: 15669097

3

Association of deletion 22 and trisomy 21: a likely random association in patients with conotruncal heart defects.

Digilio MC, Dallapiccola B, Marino B. Digilio MC, et al. Among authors: marino b. Am J Med Genet A. 2005 Apr 1;134A(1):1-2. doi: 10.1002/ajmg.a.10552. Am J Med Genet A. 2005. PMID: 15723333 No abstract available.

4

Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries.

Piacentini G, Digilio MC, Capolino R, Zorzi AD, Toscano A, Sarkozy A, D'Agostino R, Marasini M, Russo MG, Dallapiccola B, Marino B. Piacentini G, et al. Among authors: marino b. Am J Med Genet A. 2005 Aug 30;137(2):176-80. doi: 10.1002/ajmg.a.30859. Am J Med Genet A. 2005. PMID: 16059940

5

Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome).

Digilio MC, Calzolari F, Capolino R, Toscano A, Sarkozy A, de Zorzi A, Dallapiccola B, Marino B. Digilio MC, et al. Among authors: marino b. Am J Med Genet A. 2008 Jul 15;146A(14):1815-9. doi: 10.1002/ajmg.a.32407. Am J Med Genet A. 2008. PMID: 18553555

6

Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: a possible link to the Adams-Oliver syndrome.

Digilio MC, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet A. 2008 Nov 1;146A(21):2842-4. doi: 10.1002/ajmg.a.32526. Am J Med Genet A. 2008. PMID: 18924173 No abstract available.

7

16p subtelomeric duplication: a clinically recognizable syndrome.

Digilio MC, Bernardini L, Capalbo A, Capolino R, Gagliardi MG, Marino B, Novelli A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Eur J Hum Genet. 2009 Sep;17(9):1135-40. doi: 10.1038/ejhg.2009.14. Epub 2009 Mar 18. Eur J Hum Genet. 2009. PMID: 19293839 Free PMC article.

8

Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2.

Digilio MC, McDonald-McGinn DM, Heike C, Catania C, Dallapiccola B, Marino B, Zackai EH. Digilio MC, et al. Among authors: marino b. Am J Med Genet A. 2009 Dec;149A(12):2860-4. doi: 10.1002/ajmg.a.33034. Am J Med Genet A. 2009. PMID: 19890921 Free PMC article.

9

Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1.

Digilio MC, Bernardini L, Lepri F, Giuffrida MG, Guida V, Baban A, Versacci P, Capolino R, Torres B, De Luca A, Novelli A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet A. 2011 Sep;155A(9):2196-202. doi: 10.1002/ajmg.a.34131. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815254

10

Atrioventricular canal defect in patients with RASopathies.

Digilio MC, Romana Lepri F, Dentici ML, Henderson A, Baban A, Roberti MC, Capolino R, Versacci P, Surace C, Angioni A, Tartaglia M, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Eur J Hum Genet. 2013 Feb;21(2):200-4. doi: 10.1038/ejhg.2012.145. Epub 2012 Jul 11. Eur J Hum Genet. 2013. PMID: 22781091 Free PMC article.

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