Dallapiccola B - Search Results

1

Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridization.

Calabrese G, Mingarelli R, Francalanci P, Boldrini R, Palka G, Bosman C, Novelli G, Dallapiccola B. Calabrese G, et al. Among authors: dallapiccola b. Hum Genet. 1996 Apr;97(4):414-7. doi: 10.1007/BF02267058. Hum Genet. 1996. PMID: 8834234

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

The prevalence of HPV16DNA in normal and pathological cervical scrapes using the polymerase chain reaction.

Pasetto N, Sesti F, De Santis L, Piccione E, Novelli G, Dallapiccola B. Pasetto N, et al. Among authors: dallapiccola b. Gynecol Oncol. 1992 Jul;46(1):33-6. doi: 10.1016/0090-8258(92)90191-k. Gynecol Oncol. 1992. PMID: 1321780

4

Inosine-containing primers in human papillomavirus detection by polymerase chain reaction.

Novelli G, Gennarelli M, De Santis L, Angeloni P, Dallapiccola B. Novelli G, et al. Among authors: dallapiccola b. Biomed Pharmacother. 1992;46(4):167-9. doi: 10.1016/0753-3322(92)90025-3. Biomed Pharmacother. 1992. PMID: 1330051

5

Genotyping of spinal muscular atrophy families with linked DNA probes.

Gennarelli M, Melchionda S, Fattorini C, Novelli G, Dallapiccola B. Gennarelli M, et al. Among authors: dallapiccola b. Clin Genet. 1992 Dec;42(6):317-9. doi: 10.1111/j.1399-0004.1992.tb03264.x. Clin Genet. 1992. PMID: 1362926

6

Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridization.

Couillin P, Zucman J, Le Guern E, Reguigne I, Grisard MC, Delattre O, Novelli G, Dallapiccola B, Boué A. Couillin P, et al. Among authors: dallapiccola b. Ann Genet. 1992;35(3):140-5. Ann Genet. 1992. PMID: 1466562

7

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.

8

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

9

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.

10

The cystic fibrosis delta F508 mutation in the Albanian population.

Novelli G, Sangiuolo F, Mokini V, Cikuli M, Piazza A, Dallapiccola B. Novelli G, et al. Among authors: dallapiccola b. Am J Hum Genet. 1992 Apr;50(4):875-6. Am J Hum Genet. 1992. PMID: 1550133 Free PMC article. No abstract available.

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