Capolino R - Search Results

1

Confirmation of microcephaly-facio-cardio-skeletal Hadziselimovic type syndrome.

Dallapiccola B, Digilio MC, Zatterale A, Galeone R, Capolino R, Mingarelli R. Dallapiccola B, et al. Among authors: capolino r. Clin Dysmorphol. 2009 Jul;18(3):135-138. doi: 10.1097/MCD.0b013e32832a9e78. Clin Dysmorphol. 2009. PMID: 19373080

2

Transposition of the great arteries in asplenia and polysplenia phenotypes.

Marino B, Capolino R, Digilio MC, Di Donato R. Marino B, et al. Among authors: capolino r. Am J Med Genet. 2002 Jul 1;110(3):292-4. doi: 10.1002/ajmg.10376. Am J Med Genet. 2002. PMID: 12116241 No abstract available.

3

Hepatic fibrosis in Kabuki syndrome.

Nobili V, Marcellini M, Devito R, Capolino R, Viola L, Digilio MC. Nobili V, et al. Among authors: capolino r. Am J Med Genet A. 2004 Jan 15;124A(2):209-12. doi: 10.1002/ajmg.a.20387. Am J Med Genet A. 2004. PMID: 14699623

4

Polyvalvular heart disease associated with short stature, facial anomalies, and mental retardation: an additional familial report.

Digilio MC, Capolino R, Versacci P, Marino B. Digilio MC, et al. Among authors: capolino r. Am J Med Genet A. 2004 May 15;127A(1):101-103. doi: 10.1002/ajmg.a.20653. Am J Med Genet A. 2004. PMID: 15103728 No abstract available.

5

Congenital intrahepatic portosystemic venous shunt: an unusual feature in LEOPARD syndrome and in neurofibromatosis type 1.

Digilio MC, Capolino R, Marino B, Sarkozy A, Dallapiccola B. Digilio MC, et al. Among authors: capolino r. Am J Med Genet A. 2005 May 1;134(4):457-8. doi: 10.1002/ajmg.a.30582. Am J Med Genet A. 2005. PMID: 15669093 No abstract available.

6

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: capolino r. 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

7

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: capolino r. 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

8

Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of Fallot.

Vergara P, Digilio MC, De Zorzi A, Di Carlo D, Capolino R, Rimini A, Pelegrini M, Calabro R, Marino B. Vergara P, et al. Among authors: capolino r. Clin Dysmorphol. 2006 Apr;15(2):65-70. doi: 10.1097/01.mcd.0000198925.94082.ea. Clin Dysmorphol. 2006. PMID: 16531730

9

Concordant familial segregation of atrial septal defect and Axenfeld-Rieger anomaly in father and son.

Calcagni G, Digilio MC, Capolino R, Dallapiccola B, Marino B. Calcagni G, et al. Among authors: capolino r. Clin Dysmorphol. 2006 Oct;15(4):203-206. doi: 10.1097/01.mcd.0000228417.36295.4d. Clin Dysmorphol. 2006. PMID: 16957472

10

Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndrome.

Cambiaso P, Orazi C, Digilio MC, Loche S, Capolino R, Tozzi A, Faedda A, Cappa M. Cambiaso P, et al. Among authors: capolino r. J Pediatr. 2007 Jan;150(1):62-5. doi: 10.1016/j.jpeds.2006.10.060. J Pediatr. 2007. PMID: 17188616

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