Guioli S - Search Results

1

Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq.

Bardoni B, Floridia G, Guioli S, Peverali G, Anichini C, Cisternino M, Casalone R, Danesino C, Fraccaro M, Zuffardi O, et al. Bardoni B, et al. Among authors: guioli s. Hum Genet. 1993 May;91(4):333-8. doi: 10.1007/BF00217352. Hum Genet. 1993. PMID: 8099057

2

A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis.

Bardoni B, Zuffardi O, Guioli S, Ballabio A, Simi P, Cavalli P, Grimoldi MG, Fraccaro M, Camerino G. Bardoni B, et al. Among authors: guioli s. Genomics. 1991 Oct;11(2):443-51. doi: 10.1016/0888-7543(91)90153-6. Genomics. 1991. PMID: 1769656

3

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.

Bardoni B, Guioli S, Maserati E, Maraschio P, Camerino G. Bardoni B, et al. Among authors: guioli s. Hum Genet. 1988 Dec;81(1):23-5. doi: 10.1007/BF00283723. Hum Genet. 1988. PMID: 2904403

4

Kallmann syndrome due to a translocation resulting in an X/Y fusion gene.

Guioli S, Incerti B, Zanaria E, Bardoni B, Franco B, Taylor K, Ballabio A, Camerino G. Guioli S, et al. Nat Genet. 1992 Aug;1(5):337-40. doi: 10.1038/ng0892-337. Nat Genet. 1992. PMID: 1302031

5

X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region.

Mostacciuolo ML, Müller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, Camerino G, Danieli GA. Mostacciuolo ML, et al. Among authors: guioli s. Hum Genet. 1991 May;87(1):23-7. doi: 10.1007/BF01213086. Hum Genet. 1991. PMID: 1674715

6

Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and Yq.

Pedicini A, Camerino G, Avarello R, Guioli S, Zuffardi O. Pedicini A, et al. Among authors: guioli s. Genomics. 1991 Oct;11(2):482-3. doi: 10.1016/0888-7543(91)90167-d. Genomics. 1991. PMID: 1769668 No abstract available.

7

Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl.

Caiulo A, Bardoni B, Camerino G, Guioli S, Minelli A, Piantanida M, Crosato F, Dalla Fior T, Maraschio P. Caiulo A, et al. Among authors: guioli s. Hum Genet. 1989 Dec;84(1):51-4. doi: 10.1007/BF00210670. Hum Genet. 1989. PMID: 2558067

8

Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.

Guioli S, Arveiler B, Bardoni B, Notarangelo LD, Panina P, Duse M, Ugazio A, Oberlé I, de Saint Basile G, Mandel JL, et al. Guioli S, et al. Hum Genet. 1989 Dec;84(1):19-21. doi: 10.1007/BF00210664. Hum Genet. 1989. PMID: 2575070

9

A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal.

Bardoni B, Zanaria E, Guioli S, Floridia G, Worley KC, Tonini G, Ferrante E, Chiumello G, McCabe ER, Fraccaro M, et al. Bardoni B, et al. Among authors: guioli s. Nat Genet. 1994 Aug;7(4):497-501. doi: 10.1038/ng0894-497. Nat Genet. 1994. PMID: 7951319

10

Isolation and characterization of a family of sequences dispersed on the human X chromosome.

Bardoni B, Guioli S, Raimondi E, Heilig R, Mandel JL, Ottolenghi S, Camerino G. Bardoni B, et al. Among authors: guioli s. Genomics. 1988 Jul;3(1):32-8. doi: 10.1016/0888-7543(88)90155-3. Genomics. 1988. PMID: 2851539

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

35 results

Search Page

Filters