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Page 1
Peroxisomal acyl-CoA-oxidase deficiency: two new cases.
Carrozzo R, Bellini C, Lucioli S, Deodato F, Cassandrini D, Cassanello M, Caruso U, Rizzo C, Rizza T, Napolitano ML, Wanders RJ, Jakobs C, Bruno C, Santorelli FM, Dionisi-Vici C, Bonioli E. Carrozzo R, et al. Among authors: bellini c. Am J Med Genet A. 2008 Jul 1;146A(13):1676-81. doi: 10.1002/ajmg.a.32298. Am J Med Genet A. 2008. PMID: 18536048
Rubinstein-Taybi syndrome and pheochromocytoma.
Bonioli E, Bellini C. Bonioli E, et al. Among authors: bellini c. Am J Med Genet. 1992 Oct 1;44(3):386. doi: 10.1002/ajmg.1320440325. Am J Med Genet. 1992. PMID: 1488992 No abstract available.
Inheritance of Rubinstein-Taybi syndrome.
Bonioli E, Bellini C. Bonioli E, et al. Among authors: bellini c. Am J Med Genet. 1989 Apr;32(4):559. doi: 10.1002/ajmg.1320320433. Am J Med Genet. 1989. PMID: 2774008 No abstract available.
Etiology of nonimmune hydrops fetalis: a systematic review.
Bellini C, Hennekam RC, Fulcheri E, Rutigliani M, Morcaldi G, Boccardo F, Bonioli E. Bellini C, et al. Am J Med Genet A. 2009 May;149A(5):844-51. doi: 10.1002/ajmg.a.32655. Am J Med Genet A. 2009. PMID: 19334091 Review.
Sebaceous nevus syndrome: report of two cases.
Bonioli EV, Bertola A, Di Stefano A, Bellini C. Bonioli EV, et al. Among authors: bellini c. Pediatr Neurol. 1997 Jul;17(1):77-9. doi: 10.1016/s0887-8994(97)80672-8. Pediatr Neurol. 1997. PMID: 9308983
Congenital pulmonary lymphangiectasia.
Bellini C, Boccardo F, Campisi C, Bonioli E. Bellini C, et al. Orphanet J Rare Dis. 2006 Oct 30;1:43. doi: 10.1186/1750-1172-1-43. Orphanet J Rare Dis. 2006. PMID: 17074089 Free PMC article. Review.
447 results