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Page 1
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.
Cirillo E, Giardino G, Gallo V, Puliafito P, Azzari C, Bacchetta R, Cardinale F, Cicalese MP, Consolini R, Martino S, Martire B, Molinatto C, Plebani A, Scarano G, Soresina A, Cancrini C, Rossi P, Digilio MC, Pignata C. Cirillo E, et al. Among authors: digilio mc. BMC Med Genet. 2014 Jan 2;15:1. doi: 10.1186/1471-2350-15-1. BMC Med Genet. 2014. PMID: 24383682 Free PMC article.
Heterotaxia syndromes and 22q11 deletion.
Marino B, Digilio MC, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: digilio mc. 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.
Tricuspid atresia and 22q11 deletion.
Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: digilio mc. Am J Med Genet. 1997 Oct 3;72(1):40-2. doi: 10.1002/(sici)1096-8628(19971003)72:1<40::aid-ajmg8>3.0.co;2-z. Am J Med Genet. 1997. PMID: 9295072
Radial aplasia and chromosome 22q11 deletion.
Digilio MC, Giannotti A, Marino B, Guadagni AM, Orzalesi M, Dallapiccola B. Digilio MC, et al. J Med Genet. 1997 Nov;34(11):942-4. doi: 10.1136/jmg.34.11.942. J Med Genet. 1997. PMID: 9391893 Free PMC article.
Microdeletion 22q11 and oesophageal atresia.
Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B. Digilio MC, et al. J Med Genet. 1999 Feb;36(2):137-9. J Med Genet. 1999. PMID: 10051013 Free PMC article.
434 results