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For: Marino B, Digilio MC, Giannotti A, Dallapiccola B. Heterotaxia syndromes and 22q11 deletion. J Med Genet 1996;33:1052. [PMID: 9004146 DOI: 10.1136/jmg.33.12.1052] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.3] [Reference Citation Analysis]
Number Citing Articles
1 Marino B, Mileto F, Digilio MC, Carotti A, Donato RD. Congenital cardiovascular disease and velo-cardio-facial syndrome. In: Murphy KC, Scambler PJ, editors. Velo-Cardio-Facial Syndrome. Cambridge University Press; 2009. pp. 47-82. [DOI: 10.1017/cbo9780511544101.004] [Cited by in Crossref: 5] [Article Influence: 0.3] [Reference Citation Analysis]
2 Marino B, Digilio M, Toscano A. Common arterial trunk, DiGeorge syndrome and microdeletion 22q11. Progress in Pediatric Cardiology 2002;15:9-17. [DOI: 10.1016/s1058-9813(02)00004-8] [Cited by in Crossref: 12] [Article Influence: 0.6] [Reference Citation Analysis]
3 Momma K. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 2010;105:1617-24. [PMID: 20494672 DOI: 10.1016/j.amjcard.2010.01.333] [Cited by in Crossref: 153] [Cited by in F6Publishing: 113] [Article Influence: 12.8] [Reference Citation Analysis]
4 Unolt M, Versacci P, Anaclerio S, Lambiase C, Calcagni G, Trezzi M, Carotti A, Crowley TB, Zackai EH, Goldmuntz E, Gaynor JW, Digilio MC, McDonald-McGinn DM, Marino B. Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers. Am J Med Genet A 2018;176:2087-98. [PMID: 29663641 DOI: 10.1002/ajmg.a.38662] [Cited by in Crossref: 21] [Cited by in F6Publishing: 15] [Article Influence: 5.3] [Reference Citation Analysis]
5 Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B. Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2. Am J Med Genet A 2005;134A:158-64. [PMID: 15669097 DOI: 10.1002/ajmg.a.30587] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 0.7] [Reference Citation Analysis]
6 Rauch A, Hofbeck M, Leipold G, Klinge J, Trautmann U, Kirsch M, Singer H, Pfeiffer RA. Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch. Am J Med Genet 1998;78:322-31. [DOI: 10.1002/(sici)1096-8628(19980724)78:4<322::aid-ajmg4>3.0.co;2-n] [Cited by in Crossref: 47] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]