Fantasia D - Search Results

1

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. Among authors: fantasia d. Haematologica. 2002 Aug;87(8):888-9. Haematologica. 2002. PMID: 12161369 No abstract available.

2

Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb.

Calabrese G, Telvi L, Capodiferro F, Morizio E, Pizzuti A, Stuppia L, Bordoni R, Ion A, Fantasia D, Mingarelli R, Palka G. Calabrese G, et al. Among authors: fantasia d. Eur J Hum Genet. 2000 May;8(5):319-24. doi: 10.1038/sj.ejhg.5200461. Eur J Hum Genet. 2000. PMID: 10854090

3

Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping.

Calabrese G, Fantasia D, Spadano A, Morizio E, Di Bartolomeo P, Palka G. Calabrese G, et al. Among authors: fantasia d. Haematologica. 2000 Nov;85(11):1219-21. Haematologica. 2000. PMID: 11064476 No abstract available.

4

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: fantasia d. J Endocrinol Invest. 2000 Nov;23(10):659-63. doi: 10.1007/BF03343790. J Endocrinol Invest. 2000. PMID: 11097430

5

Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation.

Calabrese G, Fantasia D, Franch PG, Morizio E, Stuppia L, Gatta V, Olioso P, Mingarelli R, Spadano A, Palka G. Calabrese G, et al. Among authors: fantasia d. Bone Marrow Transplant. 2000 Nov;26(10):1125-7. doi: 10.1038/sj.bmt.1702666. Bone Marrow Transplant. 2000. PMID: 11108316

6

SHOX mutations detected by FISH and direct sequencing in patients with short stature.

Stuppia L, Calabrese G, Gatta V, Pintor S, Morizio E, Fantasia D, Guanciali Franchi P, Rinaldi MM, Scarano G, Concolino D, Giannotti A, Petreschi F, Anzellotti MT, Pomilio M, Chiarelli F, Tumini S, Palka G. Stuppia L, et al. Among authors: fantasia d. J Med Genet. 2003 Feb;40(2):E11. doi: 10.1136/jmg.40.2.e11. J Med Genet. 2003. PMID: 12566529 Free PMC article. No abstract available.

7

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: fantasia d. 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

8

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: fantasia d. 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.

9

Inositide-specific phospholipase c beta1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia.

Lo Vasco VR, Calabrese G, Manzoli L, Palka G, Spadano A, Morizio E, Guanciali-Franchi P, Fantasia D, Cocco L. Lo Vasco VR, et al. Among authors: fantasia d. Leukemia. 2004 Jun;18(6):1122-6. doi: 10.1038/sj.leu.2403368. Leukemia. 2004. PMID: 15085153

10

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: fantasia d. 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

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