Dallapiccola B - Search Results

1

Complex rearrangement of chromosomes 7q21.13-q22.1 confirms the ectrodactyly-deafness locus and suggests new candidate genes.

Bernardini L, Palka C, Ceccarini C, Capalbo A, Bottillo I, Mingarelli R, Novelli A, Dallapiccola B. Bernardini L, et al. Among authors: dallapiccola b. Am J Med Genet A. 2008 Jan 15;146A(2):238-44. doi: 10.1002/ajmg.a.32093. Am J Med Genet A. 2008. PMID: 18080328

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

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.

4

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

5

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.

6

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: dallapiccola b. Am J Med Genet. 1992 Feb 15;42(4):424-7. doi: 10.1002/ajmg.1320420404. Am J Med Genet. 1992. PMID: 1609823 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

Autosomal recessive form of whistling face syndrome in sibs.

Dallapiccola B, Giannotti A, Lembo A, Saguì L. Dallapiccola B, et al. Am J Med Genet. 1989 Aug;33(4):542-4. doi: 10.1002/ajmg.1320330426. Am J Med Genet. 1989. PMID: 2596515

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