Solé F - Search Results

1

Two cases of tetrasomy 9p syndrome with tissue limited mosaicism.

Lloveras E, Pérez C, Solé F, Zamora L, Lladonosa A, Espinet B, Silvestre E, Serra J, Vendrell T, Fernández B, Salido M, Plaja A. Lloveras E, et al. Among authors: sole f. Am J Med Genet A. 2004 Feb 1;124A(4):402-6. doi: 10.1002/ajmg.a.20447. Am J Med Genet A. 2004. PMID: 14735590

2

[Cytogenetic abnormalities in seven patients with the Sezary syndrome].

Solé F, Woessner S, Vallespí T, Domingo A, Pérez Losada A, Florensa L, Irriguible D, Espinet B, Sans-Sabrafén J. Solé F, et al. Sangre (Barc). 1995 Oct;40(5):431-3. Sangre (Barc). 1995. PMID: 8553180 Spanish.

3

[Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique].

Pérez Losada A, Solé F, Woessner S, Florensa L, Besses C, Espinet B, Caballín MR, García Eroles L, Sans-Sabrafén J. Pérez Losada A, et al. Among authors: sole f. Sangre (Barc). 1996 Jun;41(3):201-9. Sangre (Barc). 1996. PMID: 8755208 Spanish.

4

Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosis.

Solé F, de Pablos JM, Woessner S, Pérez MM, Jurado M, Espinet B, Grao P, Moratalla A, Esquivias J. Solé F, et al. Cancer Genet Cytogenet. 1997 Apr;94(2):147-50. doi: 10.1016/s0165-4608(96)00206-3. Cancer Genet Cytogenet. 1997. PMID: 9109946

5

Frequent involvement of chromosomes 1, 3, 7 and 8 in splenic marginal zone B-cell lymphoma.

Solé F, Woessner S, Florensa L, Espinet B, Mollejo M, Martín P, Piris MA. Solé F, et al. Br J Haematol. 1997 Aug;98(2):446-9. doi: 10.1046/j.1365-2141.1997.2163033.x. Br J Haematol. 1997. PMID: 9266948 Free article.

6

Two new cases of near-tetraploidy in adult acute myeloid leukemia.

Espinet B, Solé F, Woessner S, Florensa L, Besses C, Sans-Sabrafen J. Espinet B, et al. Among authors: sole f. Cancer Genet Cytogenet. 1998 Apr 15;102(2):131-4. doi: 10.1016/s0165-4608(97)00315-4. Cancer Genet Cytogenet. 1998. PMID: 9546065

7

[Priority of using conventional cytogenetics, in situ hybridization and PCR in the study of hematologic neoplasms].

Solé F, Espinet B, Woessner S. Solé F, et al. Sangre (Barc). 1998 Feb;43(1):3-5. Sangre (Barc). 1998. PMID: 9577175 Spanish. No abstract available.

8

Cytogenetic abnormalities in three patients with B-cell prolymphocytic leukemia.

Solé F, Woessner S, Espinet B, Lloveras E, Florensa L, Pérez-Losada A, Vilà RM, Besses C, Sans-Sabrafen J. Solé F, et al. Cancer Genet Cytogenet. 1998 May;103(1):43-5. doi: 10.1016/s0165-4608(97)00358-0. Cancer Genet Cytogenet. 1998. PMID: 9595043

9

[Interstitial 9q deletion: a primary change in acute non-lymphoblastic leukemia?].

Lloveras E, Solé F, Florensa L, Espinet B, Vilà RM, Besses C, Sans-Sabrafén J, Woessner S. Lloveras E, et al. Among authors: sole f. Sangre (Barc). 1998 Oct;43(5):433-5. Sangre (Barc). 1998. PMID: 9868338 Spanish.

10

Cytogenetic findings in five patients with hairy cell leukemia.

Solé F, Woessner S, Florensa L, Espinet B, Lloveras E, Pedro C, Besses C, Sabrafen JS. Solé F, et al. Cancer Genet Cytogenet. 1999 Apr;110(1):41-3. doi: 10.1016/s0165-4608(98)00178-2. Cancer Genet Cytogenet. 1999. PMID: 10198621

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