Marino B - Search Results

1

Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome.

Digilio MC, Marino B, Giannotti A, Mingarelli R, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet. 1995 Jul 31;58(1):97-8. doi: 10.1002/ajmg.1320580120. Am J Med Genet. 1995. PMID: 7573166 Review. No abstract available.

2

The atrioventricular canal defect is the congenital heart disease connecting short rib-polydactyly and oral-facial-digital syndromes.

Digilio MC, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet. 1997 Jan 10;68(1):110-2. doi: 10.1002/(sici)1096-8628(19970110)68:1<110::aid-ajmg25>3.0.co;2-w. Am J Med Genet. 1997. PMID: 8986290 No abstract available.

3

Atrioventricular canal defect without Down syndrome: a heterogeneous malformation.

Digilio MC, Marino B, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet. 1999 Jul 16;85(2):140-6. Am J Med Genet. 1999. PMID: 10406667 Review.

4

Inlet ventricular septal defect is not a partial atrioventricular septal defect.

Marino B, Digilio MC. Marino B, et al. Am J Med Genet. 1999 Nov 19;87(2):195-6. doi: 10.1002/(sici)1096-8628(19991119)87:2<195::aid-ajmg13>3.0.co;2-y. Am J Med Genet. 1999. PMID: 10533036 No abstract available.

5

Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8p.

Amati F, Mari A, Mingarelli R, Gennarelli M, Digilio MC, Giannotti A, Marino B, Novelli G, Dallapiccola B. Amati F, et al. Among authors: marino b. Am J Med Genet. 1995 Jul 3;57(3):483-8. doi: 10.1002/ajmg.1320570325. Am J Med Genet. 1995. PMID: 7677156

6

Atrioventricular canal and 8p- syndrome.

Digilio MC, Giannotti A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet. 1993 Sep 1;47(3):437-8. doi: 10.1002/ajmg.1320470331. Am J Med Genet. 1993. PMID: 8135296 Review. No abstract available.

7

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.

8

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.

9

Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: a specific cardiac phenotype associated with deletion 18q syndrome.

Versacci P, Digilio MC, Sauer U, Dallapiccola B, Marino B. Versacci P, et al. Among authors: marino b. Am J Med Genet A. 2005 Oct 1;138A(2):185-6. doi: 10.1002/ajmg.a.30916. Am J Med Genet A. 2005. PMID: 16100728 No abstract available.

10

CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects.

Sarkozy A, Esposito G, Conti E, Digilio MC, Marino B, Calabrò R, Pizzuti A, Dallapiccola B. Sarkozy A, et al. Among authors: marino b. Am J Med Genet A. 2005 Dec 15;139(3):236-8. doi: 10.1002/ajmg.a.31018. Am J Med Genet A. 2005. PMID: 16278904 No abstract available.

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