Publicaciones en las que colabora con CONCEPCION LOPEZ GINES (27)

2007

  1. Concurrent EGFR amplification and TP-53 mutation in glioblastomas

    Clinical Neuropathology, Vol. 26, Núm. 5, pp. 224-231

2006

  1. Desmoplastic infantile ganglioglioma. Morphological, immunohistochemical and genetic features [8]

    Histopathology

  2. Primary glioblastoma with EGFR amplification and a ring chromosome 7 in a young patient

    Clinical Neuropathology, Vol. 25, Núm. 4, pp. 193-199

  3. Solitary fibrous tumor of the orbit: Morphological, cytogenetic and molecular features

    Neuropathology, Vol. 26, Núm. 6, pp. 557-563

2005

  1. Association of chromosome 7, chromosome 10 and EGFR gene amplification in glioblastoma multiforme

    Clinical Neuropathology, Vol. 24, Núm. 5, pp. 209-218

2004

  1. Deregulation of the G1 to S-phase cell cycle checkpoint is involved in the pathogenesis of human osteosarcoma

    Diagnostic Molecular Pathology, Vol. 13, Núm. 2, pp. 81-91

2003

  1. Cytogenetic and molecular findings related to rhabdomyosarcoma. An analysis of seven cases

    Cancer Genetics and Cytogenetics, Vol. 144, Núm. 2, pp. 125-133

  2. Establishment and characterization of a continuous human chondrosarcoma cell line, ch-2879: Comparative histologic and genetic studies with its tumor of origin

    Laboratory Investigation, Vol. 83, Núm. 6, pp. 877-887

1998

  1. New type of chimeric fusion product between the EWS and ATFI genes in clear cell sarcoma (malignant melanoma of soft parts)

    Genes Chromosomes and Cancer, Vol. 23, Núm. 4, pp. 358-360

  2. Primary rhabdomyosarcoma mimicking a small cell sarcoma of bone: A nude mice xenograft, cytogenetic, and molecular approach

    International Journal of Surgical Pathology, Vol. 6, Núm. 2, pp. 61-72

1992

  1. Cytogenetics, flow cytometry, cytophotometry and morphometry of 22 cases of primary breast carcinoma - A comparative study

    Virchows Archiv B Cell Pathology Including Molecular Pathology, Vol. 61, Núm. 1, pp. 133-140

1991

  1. 45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome

    Revista clínica española, Vol. 189, Núm. 1, pp. 23-25

  2. CROMOSOMA 22 EN ANILLO. DESCRIPCION DE UN NUEVO CASO (1)

    Anales Espanoles de Pediatria, Vol. 35, Núm. 1, pp. 62-64

1990

  1. Dos nuevos casos de translocación Y-autosoma asociada con azoospermia.

    Revista clinica espanola, Vol. 187, Núm. 2, pp. 71-73

1989

  1. An unusual translocation associated with recurrent spontaneous abortions

    Human Genetics, Vol. 83, Núm. 2, pp. 202

  2. Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21)

    Human Genetics, Vol. 83, Núm. 2, pp. 203

  3. Malignant myxoid liposarcoma: An immunohistochemical, electron-microscopical and cytogenetical analysis

    Applied Pathology, Vol. 7, Núm. 5, pp. 285-293

  4. Resultados citogenéticos en nueve casos de linfomas no-Hodgkin de alto grado de malignidad.

    Sangre, Vol. 34, Núm. 4, pp. 278-284

  5. TRANSLOCACION FAMILIAR t(9; 10) (q34; q22) DETECTADA EN UN NINO PORTADOR CON ALGUNAS ANOMALIAS FENOTIPICAS

    Anales Espanoles de Pediatria, Vol. 31, Núm. 5, pp. 481-482

1988

  1. Letter to the editor: Translocation (X;18) in a synovial sarcoma: A new case

    Cancer Genetics and Cytogenetics