Morizio E - Search Results

1

Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene.

Stuppia L, Gatta V, Scarciolla O, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Among authors: morizio e. Genomics. 2005 Feb;85(2):280-3. doi: 10.1016/j.ygeno.2004.10.015. Genomics. 2005. PMID: 15676287

2

Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene.

Stuppia L, Gatta V, Fogh I, Gaspari AR, Morizio E, Mingarelli R, Di Santo M, Pizzuti A, Calabrese G, Palka G. Stuppia L, et al. Among authors: morizio e. Genomics. 2001 Mar 1;72(2):153-7. doi: 10.1006/geno.2001.6450. Genomics. 2001. PMID: 11401428

3

A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient.

Pizzuti A, Calabrese G, Bozzali M, Telvi L, Morizio E, Guida V, Gatta V, Stuppia L, Ion A, Palka G, Dallapiccola B. Pizzuti A, et al. Among authors: morizio e. Invest Ophthalmol Vis Sci. 2002 Dec;43(12):3609-12. Invest Ophthalmol Vis Sci. 2002. PMID: 12454025

4

Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts (RAEB).

Calabrese G, Fantasia D, Morizio E, Toro PM, Franchi PG, Fornaro A, Spadano A, Stuppia L, Palka G. Calabrese G, et al. Among authors: morizio e. Br J Haematol. 2003 Sep;122(5):760-3. doi: 10.1046/j.1365-2141.2003.04493.x. Br J Haematol. 2003. PMID: 12930385 Free article.

5

Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay.

Gatta V, Antonucci I, Morizio E, Palka C, Fischetto R, Mokini V, Tumini S, Calabrese G, Stuppia L. Gatta V, et al. Among authors: morizio e. J Hum Genet. 2007;52(1):21-27. doi: 10.1007/s10038-006-0074-5. Epub 2006 Nov 8. J Hum Genet. 2007. PMID: 17091221

6

Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.

Palka C, Alfonsi M, Mohn A, Cerbo R, Guanciali Franchi P, Fantasia D, Morizio E, Stuppia L, Calabrese G, Zori R, Chiarelli F, Palka G. Palka C, et al. Among authors: morizio e. Pediatrics. 2012 Jan;129(1):e183-8. doi: 10.1542/peds.2010-2094. Epub 2011 Dec 5. Pediatrics. 2012. PMID: 22144704

7

Assignment of the beta-arrestin 1 gene (ARRB1) to human chromosome 11q13.

Calabrese G, Sallese M, Stornaiuolo A, Morizio E, Palka G, De Blasi A. Calabrese G, et al. Among authors: morizio e. Genomics. 1994 Nov 1;24(1):169-71. doi: 10.1006/geno.1994.1594. Genomics. 1994. PMID: 7896272

8

Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene.

Stuppia L, Gatta V, Mastroprimiano G, Pompetti F, Calabrese G, Guanciali Franchi P, Morizio E, Mingarelli R, Nicolai M, Tenaglia R, Improta L, Sforza V, Bisceglia S, Palka G. Stuppia L, et al. Among authors: morizio e. J Med Genet. 1997 Nov;34(11):881-3. doi: 10.1136/jmg.34.11.881. J Med Genet. 1997. PMID: 9391878 Free PMC article.

9

FISH analysis in detecting 9p duplication (p22p24).

Guanciali Franchi P, Calabrese G, Morizio E, Modestini E, Stuppia L, Mingarelli R, Palka G. Guanciali Franchi P, et al. Among authors: morizio e. Am J Med Genet. 2000 Jan 3;90(1):35-7. Am J Med Genet. 2000. PMID: 10602115

10

Characterization of novel genes in AZF regions.

Stuppia L, Gatta V, Fogh I, Gaspari AR, Grande R, Morizio E, Fantasia D, Pizzuti A, Calabrese G, Palka G. Stuppia L, et al. Among authors: morizio e. J Endocrinol Invest. 2000 Nov;23(10):659-63. doi: 10.1007/BF03343790. J Endocrinol Invest. 2000. PMID: 11097430

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