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977 results

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Page 1
Pure trisomy 19p syndrome in an infant with an extra ring chromosome.
Novelli A, Ceccarini C, Bernardini L, Zuccarello D, Digilio MC, Mingarelli R, Dallapiccola B. Novelli A, et al. Among authors: dallapiccola b. Cytogenet Genome Res. 2005;111(2):182-5. doi: 10.1159/000086391. Cytogenet Genome Res. 2005. PMID: 16103663
Horseshoe lung: an additional component of the Vater association.
Obregon MG, Giannotti A, Digilio MC, Barbuti D, Mingarelli R, Dallapiccola B. Obregon MG, et al. Among authors: dallapiccola b. Pediatr Radiol. 1992;22(2):158. doi: 10.1007/BF02011329. Pediatr Radiol. 1992. PMID: 1307865 No abstract available.
Familial postaxial acrofacial dysostosis syndrome.
Giannotti A, Digilio MC, Virgili Q, Obregon MG, Guadagni AM, Ventura T, Dallapiccola B. Giannotti A, et al. Among authors: dallapiccola b. J Med Genet. 1992 Oct;29(10):752. doi: 10.1136/jmg.29.10.752. J Med Genet. 1992. PMID: 1433242 Free PMC article. No abstract available.
Radiographic findings in Wiedemann-Rautenstrauch syndrome.
Obregon MG, Bergami GL, Giannotti A, Digilio MC, Virgili Q, Guadagni AM, Pompei E, Dallapiccola B. Obregon MG, et al. Among authors: dallapiccola b. Pediatr Radiol. 1992;22(6):474-5. doi: 10.1007/BF02013521. Pediatr Radiol. 1992. PMID: 1437383
Partial deletion 10p syndrome. Report of two patients.
Obregon MG, Mingarelli R, Giannotti A, di Comite A, Spedicato FS, Dallapiccola B. Obregon MG, et al. Among authors: dallapiccola b. Ann Genet. 1992;35(2):101-4. Ann Genet. 1992. PMID: 1524405
977 results