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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Sandrin-Garcia P, Macedo C, Martelli LR, Ramos ES, Guion-Almeida ML, Richieri-Costa A, Passos GA. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clin Genet 2002;61:380-3. [PMID: 12081724 DOI: 10.1034/j.1399-0004.2002.610511.x] [Cited by in Crossref: 32] [Cited by in F6Publishing: 29] [Article Influence: 1.6] [Reference Citation Analysis]
2 Rosa RFM, Zen PRG, Graziadio C, Paskulin GA. Síndrome de deleção 22q11.2 e cardiopatias congênitas. Rev paul pediatr 2011;29:251-60. [DOI: 10.1590/s0103-05822011000200018] [Cited by in Crossref: 5] [Article Influence: 0.5] [Reference Citation Analysis]