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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: giannotti a. Pediatr Radiol. 1992;22(2):158. doi: 10.1007/BF02011329. Pediatr Radiol. 1992. PMID: 1307865 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: giannotti a. Pediatr Radiol. 1992;22(6):474-5. doi: 10.1007/BF02013521. Pediatr Radiol. 1992. PMID: 1437383
Turner's syndrome with atrioventricular canal.
Marino B, Digilio MC, Papa M, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: giannotti a. Pediatr Cardiol. 1991 Oct;12(4):245-6. doi: 10.1007/BF02310577. Pediatr Cardiol. 1991. PMID: 1946018 No abstract available.
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: giannotti a. Ann Genet. 1992;35(2):101-4. Ann Genet. 1992. PMID: 1524405
Interstitial deletion del(17) (q21.3q23 or 24.2) syndrome.
Dallapiccola B, Mingarelli R, Digilio C, Obregon MG, Giannotti A. Dallapiccola B, et al. Among authors: giannotti a. Clin Genet. 1993 Jan;43(1):54-5. doi: 10.1111/j.1399-0004.1993.tb04452.x. Clin Genet. 1993. PMID: 8462199 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. 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.
149 results