Camerino G - Search Results

1

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: camerino g. Genomics. 1991 Oct;11(2):443-51. doi: 10.1016/0888-7543(91)90153-6. Genomics. 1991. PMID: 1769656

2

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: camerino g. Genomics. 1991 Oct;11(2):482-3. doi: 10.1016/0888-7543(91)90167-d. Genomics. 1991. PMID: 1769668 No abstract available.

3

Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this region.

Ballabio A, Bardoni B, Guioli S, Basler E, Camerino G. Ballabio A, et al. Among authors: camerino g. Genomics. 1990 Oct;8(2):263-70. doi: 10.1016/0888-7543(90)90281-x. Genomics. 1990. PMID: 2249849

4

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: camerino g. Genomics. 1988 Jul;3(1):32-8. doi: 10.1016/0888-7543(88)90155-3. Genomics. 1988. PMID: 2851539

5

A new submicroscopic deletion that refines the 9p region for sex reversal.

Calvari V, Bertini V, De Grandi A, Peverali G, Zuffardi O, Ferguson-Smith M, Knudtzon J, Camerino G, Borsani G, Guioli S. Calvari V, et al. Among authors: camerino g. Genomics. 2000 May 1;65(3):203-12. doi: 10.1006/geno.2000.6160. Genomics. 2000. PMID: 10857744

6

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. Among authors: camerino g. Nat Genet. 1992 Aug;1(5):337-40. doi: 10.1038/ng0892-337. Nat Genet. 1992. PMID: 1302031

7

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: camerino g. Hum Genet. 1991 May;87(1):23-7. doi: 10.1007/BF01213086. Hum Genet. 1991. PMID: 1674715

8

Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23.

Caiulo A, Nicolis S, Bianchi P, Zuffardi O, Bardoni B, Maraschio P, Ottolenghi S, Camerino G, Giglioni B. Caiulo A, et al. Among authors: camerino g. Hum Genet. 1991 Feb;86(4):388-90. doi: 10.1007/BF00201840. Hum Genet. 1991. PMID: 1999341

9

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: camerino g. Hum Genet. 1989 Dec;84(1):51-4. doi: 10.1007/BF00210670. Hum Genet. 1989. PMID: 2558067

10

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: camerino g. Hum Genet. 1988 Dec;81(1):23-5. doi: 10.1007/BF00283723. Hum Genet. 1988. PMID: 2904403

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