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977 results

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Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome.
Digilio MC, Marino B, Giannotti A, Mingarelli R, Dallapiccola B. Digilio MC, et al. Among authors: dallapiccola b. Am J Med Genet. 1995 Jul 31;58(1):97-8. doi: 10.1002/ajmg.1320580120. Am J Med Genet. 1995. PMID: 7573166 Review. No abstract available.
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