Calabrese G - Search Results

1

Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis.

Guanciali-Franchi P, Calabrese G, Morizio E, Fantasia D, Colosimo A, Rinaldi MM, Cristini L, Simonelli A, Lonardo F, Turci A, Zatterale A, Laganà C, Stuppia L, Sabatino G, Palka G. Guanciali-Franchi P, et al. Among authors: calabrese g. Am J Med Genet A. 2004 Jun 1;127A(2):144-8. doi: 10.1002/ajmg.a.20691. Am J Med Genet A. 2004. PMID: 15108201

2

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. 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.

3

A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.

Guanciali-Franchi P, Calabrese G, Morizio E, Gatta V, Palka C, Stuppia L, Zuffardi O. Guanciali-Franchi P, et al. Among authors: calabrese g. Eur J Med Genet. 2008 May-Jun;51(3):239-44. doi: 10.1016/j.ejmg.2008.02.002. Epub 2008 Feb 13. Eur J Med Genet. 2008. PMID: 18378203

4

Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis.

Calabrese G, Stuppia L, Mingarelli R, Guanciali Franchi P, Peila R, Morizio E, Antonucci A, Palka G. Calabrese G, et al. Ann Genet. 1994;37(3):135-8. Ann Genet. 1994. PMID: 7847794

5

A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn female.

Palka G, Calabrese G, Stuppia L, Guanciali Franchi P, Morizio E, Peila R, Antonucci A. Palka G, et al. Among authors: calabrese g. Clin Genet. 1994 Feb;45(2):93-6. doi: 10.1111/j.1399-0004.1994.tb04001.x. Clin Genet. 1994. PMID: 8004805

6

Duplication Xp22.2 and pseudoisodicentric Yq detected by FISH and PCR in a sterile male.

Palka G, Calabrese G, Mingarelli R, Guanciali Franchi P, Stuppia L, Morizio E, Peila R, Antonucci A. Palka G, et al. Among authors: calabrese g. Clin Genet. 1995 Oct;48(4):213-6. doi: 10.1111/j.1399-0004.1995.tb04091.x. Clin Genet. 1995. PMID: 8591674

7

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: calabrese g. Am J Med Genet. 2000 Jan 3;90(1):35-7. Am J Med Genet. 2000. PMID: 10602115

8

Deletion of the SHOX gene in patients with short stature of unknown cause.

Morizio E, Stuppia L, Gatta V, Fantasia D, Guanciali Franchi P, Rinaldi MM, Scarano G, Concolino D, Giannotti A, Verrotti A, Chiarelli F, Calabrese G, Palka G. Morizio E, et al. Among authors: calabrese g. Am J Med Genet A. 2003 Jun 15;119A(3):293-6. doi: 10.1002/ajmg.a.20198. Am J Med Genet A. 2003. PMID: 12784295

9

Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia.

Calabrese G, Taraborelli T, Fantasia D, Guanciali Franchi P, Spadano A, Palka G. Calabrese G, et al. Haematologica. 2002 Aug;87(8):888-9. Haematologica. 2002. PMID: 12161369 No abstract available.

10

Cytogenetic survey of 80 patients with acute nonlymphocytic leukemia.

Palka G, Calabrese G, Fioritoni G, Stuppia L, Guanciali Franchi P, Marino M, Antonucci A, Spadano A, Torlontano G. Palka G, et al. Among authors: calabrese g. Cancer Genet Cytogenet. 1992 Mar;59(1):45-50. doi: 10.1016/0165-4608(92)90156-3. Cancer Genet Cytogenet. 1992. PMID: 1555190

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