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143 results
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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
Heterotaxia syndromes and 22q11 deletion.
Marino B, Digilio MC, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: giannotti a. J Med Genet. 1996 Dec;33(12):1052. doi: 10.1136/jmg.33.12.1052. J Med Genet. 1996. PMID: 9004146 Free PMC article. No abstract available.
Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome.
Digilio MC, Marino B, Giannotti A, Mingarelli R, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. 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.
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.
Heterotaxy with left atrial isomerism in a patient with deletion 18p.
Digilio MC, Marino B, Giannotti A, Di Donato R, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am J Med Genet. 2000 Sep 18;94(3):198-200. doi: 10.1002/1096-8628(20000918)94:3<198::aid-ajmg4>3.0.co;2-9. Am J Med Genet. 2000. PMID: 10995505
143 results