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953 results

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Page 1
Atrioventricular canal defect in patients with RASopathies.
Digilio MC, Romana Lepri F, Dentici ML, Henderson A, Baban A, Roberti MC, Capolino R, Versacci P, Surace C, Angioni A, Tartaglia M, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Eur J Hum Genet. 2013 Feb;21(2):200-4. doi: 10.1038/ejhg.2012.145. Epub 2012 Jul 11. Eur J Hum Genet. 2013. PMID: 22781091 Free PMC article.
Genetics of atrioventricular canal defects.
Pugnaloni F, Digilio MC, Putotto C, De Luca E, Marino B, Versacci P. Pugnaloni F, et al. Among authors: marino b. Ital J Pediatr. 2020 May 13;46(1):61. doi: 10.1186/s13052-020-00825-4. Ital J Pediatr. 2020. PMID: 32404184 Free PMC article. Review.
Tricuspid atresia and 22q11 deletion.
Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B. Marino B, et al. 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. Among authors: marino b. 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.
Congenital heart defect in sibs with discordant karyotypes.
Digilio MC, Marino B, Canepa SA, Borzaga U, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet. 1998 Nov 2;80(2):169-72. doi: 10.1002/(sici)1096-8628(19981102)80:2<169::aid-ajmg15>3.0.co;2-e. Am J Med Genet. 1998. PMID: 9805136
Microdeletion 22q11 and oesophageal atresia.
Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. J Med Genet. 1999 Feb;36(2):137-9. J Med Genet. 1999. PMID: 10051013 Free PMC article.
953 results