Dallapiccola B - Search Results

1

Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells.

Massari A, Novelli G, Colosimo A, Sangiuolo F, Palka G, Calabrese G, Camurri L, Ghirardini G, Milani G, Giorlandino C, Gazzanelli G, Malatesta M, Romanini C, Dallapiccola B. Massari A, et al. Among authors: dallapiccola b. Hum Genet. 1996 Feb;97(2):150-5. doi: 10.1007/BF02265257. Hum Genet. 1996. PMID: 8566945

2

Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

Pizzuti A, Novelli G, Mari A, Ratti A, Colosimo A, Amati F, Penso D, Sangiuolo F, Calabrese G, Palka G, Silani V, Gennarelli M, Mingarelli R, Scarlato G, Scambler P, Dallapiccola B. Pizzuti A, et al. Among authors: dallapiccola b. Am J Hum Genet. 1996 Apr;58(4):722-9. Am J Hum Genet. 1996. PMID: 8644734 Free PMC article.

3

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

4

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

5

Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13.

Novelli G, Capon F, Tamisari L, Grandi E, Angelini C, Guerrini P, Dallapiccola B. Novelli G, et al. Among authors: dallapiccola b. J Med Genet. 1995 Mar;32(3):216-9. doi: 10.1136/jmg.32.3.216. J Med Genet. 1995. PMID: 7783173 Free PMC article.

6

A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patients.

Capon F, Melchionda S, Gennarelli M, Lo Cicero S, Giacanelli M, Novelli G, Dallapiccola B. Capon F, et al. Among authors: dallapiccola b. Mol Cell Probes. 1993 Jun;7(3):221-6. doi: 10.1006/mcpr.1993.1032. Mol Cell Probes. 1993. PMID: 8366867

7

cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene.

Pizzuti A, Amati F, Calabrese G, Mari A, Colosimo A, Silani V, Giardino L, Ratti A, Penso D, Calzà L, Palka G, Scarlato G, Novelli G, Dallapiccola B. Pizzuti A, et al. Among authors: dallapiccola b. Hum Mol Genet. 1996 Jul;5(7):953-8. doi: 10.1093/hmg/5.7.953. Hum Mol Genet. 1996. PMID: 8817329

8

Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassay.

Colosimo A, Novelli G, Cavicchini A, Dallapiccola B. Colosimo A, et al. Among authors: dallapiccola b. Int J Clin Lab Res. 1996;26(2):136-9. doi: 10.1007/BF02592357. Int J Clin Lab Res. 1996. PMID: 8856368

9

Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization.

Colosimo A, Calabrese G, Gennarelli M, Ruzzo AM, Sangiuolo F, Magnani M, Palka G, Novelli G, Dallapiccola B. Colosimo A, et al. Among authors: dallapiccola b. Cytogenet Cell Genet. 1996;74(3):187-8. doi: 10.1159/000134409. Cytogenet Cell Genet. 1996. PMID: 8941369 No abstract available.

10

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.

Pizzuti A, Novelli G, Ratti A, Amati F, Mari A, Calabrese G, Nicolis S, Silani V, Marino B, Scarlato G, Ottolenghi S, Dallapiccola B. Pizzuti A, et al. Among authors: dallapiccola b. Hum Mol Genet. 1997 Feb;6(2):259-65. doi: 10.1093/hmg/6.2.259. Hum Mol Genet. 1997. PMID: 9063746

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