Dallapiccola B - Search Results

1

Gingival overgrowth, congenital generalized hypertrichosis, mental retardation and epilepsy: case report and overview.

Douzgou S, Mingarelli R, Dallapiccola B. Douzgou S, et al. Among authors: dallapiccola b. Clin Dysmorphol. 2009 Oct;18(4):205-8. doi: 10.1097/MCD.0b013e32832dc393. Clin Dysmorphol. 2009. PMID: 19625955 Review.

2

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: dallapiccola b. Ann Genet. 1992;35(4):208-12. Ann Genet. 1992. PMID: 1296516

3

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.

4

Comment on the paper of Qumsiyeh et al. (Am J Med Genet 41: 99-101, 1991).

Zelante L, Mingarelli R, Dallapiccola B. Zelante L, et al. Among authors: dallapiccola b. Am J Med Genet. 1992 Dec 1;44(6):844-6. doi: 10.1002/ajmg.1320440630. Am J Med Genet. 1992. PMID: 1481861 No abstract available.

5

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

6

Baller-Gerold syndrome: case report and clinical and radiological review.

Dallapiccola B, Zelante L, Mingarelli R, Pellegrino M, Bertozzi V. Dallapiccola B, et al. Am J Med Genet. 1992 Feb 1;42(3):365-8. doi: 10.1002/ajmg.1320420323. Am J Med Genet. 1992. PMID: 1536180 Review.

7

Acromegaloid facial appearance (AFA) syndrome: report of a second family.

Dallapiccola B, Zelante L, Accadia L, Mingarelli R. Dallapiccola B, et al. J Med Genet. 1992 Jun;29(6):419-22. doi: 10.1136/jmg.29.6.419. J Med Genet. 1992. PMID: 1619638 Free PMC article.

8

Ring chromosome 8 associated with microcephaly.

Mingarelli R, Valorani G, Zelante L, Dallapiccola B. Mingarelli R, et al. Among authors: dallapiccola b. Ann Genet. 1991;34(2):90-2. Ann Genet. 1991. PMID: 1746890

9

Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and review.

Zelante L, Torricelli F, Calvano S, Mingarelli R, Dallapiccola B. Zelante L, et al. Among authors: dallapiccola b. Ann Genet. 1991;34(2):93-7. Ann Genet. 1991. PMID: 1746891 Review.

10

Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

Mari A, Amati F, Mingarelli R, Giannotti A, Sebastio G, Colloridi V, Novelli G, Dallapiccola B. Mari A, et al. Among authors: dallapiccola b. Hum Genet. 1995 Oct;96(4):444-8. doi: 10.1007/BF00191804. Hum Genet. 1995. PMID: 7557968

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