Giannotti A - Search Results

1

Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.

Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B. Obregon MG, et al. Among authors: giannotti a. Ann Genet. 1992;35(4):208-12. Ann Genet. 1992. PMID: 1296516

2

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

3

Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter).

Calabrese G, Giannotti A, Mingarelli R, Di Gilio MC, Piemontese MR, Palka G. Calabrese G, et al. Among authors: giannotti a. Clin Genet. 1997 Apr;51(4):264-7. Clin Genet. 1997. PMID: 9184250

4

Radial aplasia and chromosome 22q11 deletion.

Digilio MC, Giannotti A, Marino B, Guadagni AM, Orzalesi M, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. 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.

5

Langer-Giedion syndrome. A patient without mental retardation and a large 8q23.2-q24.22 deletion.

Tiberio G, Digilio MC, Giannotti A. Tiberio G, et al. Among authors: giannotti a. Minerva Pediatr. 1999 Sep-Oct;51(9-10):313-8. Minerva Pediatr. 1999. PMID: 10783592 Review. English, Italian.

6

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.

7

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

8

[Partial deletion of the long arm of chromosome 17. Presentation of a clinical case].

Giannotti A, Alessandri A, Reale A, Digilio MC, Valorani MG. Giannotti A, et al. Minerva Pediatr. 1992 Jan-Feb;44(1-2):51-4. Minerva Pediatr. 1992. PMID: 1552879 Italian.

9

Nonrandom association of atrioventricular canal and del (8p) syndrome.

Marino B, Reale A, Giannotti A, Digilio MC, Dallapiccola B. Marino B, et al. Among authors: giannotti a. Am J Med Genet. 1992 Feb 15;42(4):424-7. doi: 10.1002/ajmg.1320420404. Am J Med Genet. 1992. PMID: 1609823 Review.

10

New case of Bartsocas-Papas syndrome surviving at 20 months.

Giannotti A, Digilio MC, Standoli L, Zama M, Dallapiccola B. Giannotti A, et al. Am J Med Genet. 1992 Mar 1;42(5):733-5. doi: 10.1002/ajmg.1320420522. Am J Med Genet. 1992. PMID: 1632449

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