Giglio S - Search Results

1

Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation.

Giglio S, Calvari V, Gregato G, Gimelli G, Camanini S, Giorda R, Ragusa A, Guerneri S, Selicorni A, Stumm M, Tonnies H, Ventura M, Zollino M, Neri G, Barber J, Wieczorek D, Rocchi M, Zuffardi O. Giglio S, et al. Am J Hum Genet. 2002 Aug;71(2):276-85. doi: 10.1086/341610. Epub 2002 Jun 10. Am J Hum Genet. 2002. PMID: 12058347 Free PMC article.

2

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

Banfi S, Borsani G, Rossi E, Bernard L, Guffanti A, Rubboli F, Marchitiello A, Giglio S, Coluccia E, Zollo M, Zuffardi O, Ballabio A. Banfi S, et al. Among authors: giglio s. Nat Genet. 1996 Jun;13(2):167-74. doi: 10.1038/ng0696-167. Nat Genet. 1996. PMID: 8640222

3

Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?

Piantanida M, Dellavecchia C, Floridia G, Giglio S, Hoeller H, Dordi B, Danesino C, Schinzel A, Zuffardi O. Piantanida M, et al. Among authors: giglio s. Hum Genet. 1997 Jun;99(6):766-71. doi: 10.1007/s004390050445. Hum Genet. 1997. PMID: 9187670

4

Ring chromosome 13 with loss of the region D13S317-D13S285: phenotypic overlap with XK syndrome.

Guala A, Dellavecchia C, Mannarino S, Rognone F, Giglio S, Minelli A, Danesino C. Guala A, et al. Among authors: giglio s. Am J Med Genet. 1997 Oct 31;72(3):319-23. Am J Med Genet. 1997. PMID: 9332662 Review.

5

Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25.

Pirola B, Bortotto L, Giglio S, Piovan E, Janes A, Guerrini R, Zuffardi O. Pirola B, et al. Among authors: giglio s. J Med Genet. 1998 Dec;35(12):1031-3. doi: 10.1136/jmg.35.12.1031. J Med Genet. 1998. PMID: 9863602 Free PMC article.

6

Transmission of a fully functional human neocentromere through three generations.

Tyler-Smith C, Gimelli G, Giglio S, Floridia G, Pandya A, Terzoli G, Warburton PE, Earnshaw WC, Zuffardi O. Tyler-Smith C, et al. Among authors: giglio s. Am J Hum Genet. 1999 May;64(5):1440-4. doi: 10.1086/302380. Am J Hum Genet. 1999. PMID: 10205277 Free PMC article.

7

Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes.

Fogli A, Giglio S, Arrigo G, Lo Nigro C, Zollo M, Viggiano L, Rocchi M, Archidiacono N, Zuffardi O, Carrozzo R. Fogli A, et al. Among authors: giglio s. Cytogenet Cell Genet. 1999;86(3-4):225-32. doi: 10.1159/000015344. Cytogenet Cell Genet. 1999. PMID: 10575211

8

Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.

Giglio S, Pirola B, Arrigo G, Dagrada P, Bardoni B, Bernardi F, Russo G, Argentiero L, Forabosco A, Carrozzo R, Zuffardi O. Giglio S, et al. Eur J Hum Genet. 2000 Jan;8(1):63-70. doi: 10.1038/sj.ejhg.5200394. Eur J Hum Genet. 2000. PMID: 10713889

9

Genomic organization and chromosomal localization of the mouse Connexin36 (mCx36) gene.

Cicirata F, Parenti R, Spinella F, Giglio S, Tuorto F, Zuffardi O, Gulisano M. Cicirata F, et al. Among authors: giglio s. Gene. 2000 Jun 27;251(2):123-30. doi: 10.1016/s0378-1119(00)00202-x. Gene. 2000. PMID: 10876089

10

Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12.

Bardoni B, Giglio S, Schenck A, Rocchi M, Mandel JL. Bardoni B, et al. Among authors: giglio s. Cytogenet Cell Genet. 2000;89(1-2):11-3. doi: 10.1159/000015580. Cytogenet Cell Genet. 2000. PMID: 10894927 No abstract available.

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