Publicaciones (86) Publicaciones en las que ha participado algún/a investigador/a

2005

  1. A novel insertion in the <i>FGFR2</i> gene in a patient with Crouzon phenotype and sacrococcygeal tail

    BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

  2. A novel insertion in the FGFR2 gene in a patient with Crouzon phenotype and sacrococcygeal tail

    Birth Defects Research Part A - Clinical and Molecular Teratology, Vol. 73, Núm. 1, pp. 61-64

  3. Adaptación de un diseño de planificación tradicional a un equipo alevín de natación sincronizada.

    Comunicaciones técnicas, Núm. 3, pp. 43

  4. Alagille syndrome: Cutaneous manifestations in 38 children

    Pediatric Dermatology, Vol. 22, Núm. 1, pp. 11-14

  5. Alternativas al calostro

    Bovis, Núm. 122, pp. 57-62

  6. Amadori adducts activate nuclear factor-κB-related proinflammatory genes in cultured human peritoneal mesothelial cells

    British Journal of Pharmacology, Vol. 146, Núm. 2, pp. 268-279

  7. An experimental study of cooperation in a natural setting

    Revista mexicana de análisis de la conducta = Mexican journal of behavior analysis, Vol. 31, Núm. 2, pp. 261-281

  8. Anti-glucuronoxylomannan IgG1 specific antibodies production in Cryptococcus neoformans resistant mice.

    Biomédica : revista del Instituto Nacional de Salud, Vol. 25, Núm. 1, pp. 110-119

  9. Antimuscarinic agents exhibit local inhibitory effects on muscarinic receptors in bladder-afferent pathways

    Urology, Vol. 65, Núm. 2, pp. 238-242

  10. Análisis de las interacciones que tienen lugar entre un grupo de investigadores, al llevar a cabo un experimento: datos preliminares

    Avances en la Investigación Científica (Universidad de Guadalajara), pp. 437-442

  11. Análisis de las interacciones que tuvieron lugar entre los miembros de un grupo de investigación, durante el desarrollo de un experimento: datos preliminares

    Avances en la Investigación Científica (Universidad de Guadalajara), pp. 424-429

  12. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y

    European Journal of Medical Genetics, Vol. 48, Núm. 2, pp. 159-166

  13. Cardiac rupture during contrast-enhanced dobutamine stress echocardiography

    International Journal of Cardiology, Vol. 98, Núm. 2, pp. 349-350

  14. Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndrome

    American Journal of Medical Genetics, Vol. 138 A, Núm. 3, pp. 272-277

  15. Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome

    Clinical Genetics, Vol. 68, Núm. 4, pp. 373-378

  16. Comparison of the NEO-FFI, the NEO-FFI-R and an alternative short version of the NEO-PI-R (NEO-60) in Swiss and Spanish samples

    Personality and Individual Differences, Vol. 38, Núm. 3, pp. 591-604

  17. Cooperative story telling in the “Story Table” environment

    7th Alps-Adria Conference in Psychology,

  18. Craniofacial dyssynostosis: Description of the first four Spanish cases and review

    American Journal of Medical Genetics, Vol. 132 A, Núm. 1, pp. 41-48

  19. Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome

    American Journal of Human Genetics, Vol. 77, Núm. 2, pp. 205-218

  20. Detection of human immunodeficiency virus type 1 RNA by in situ hybridization in oral mucosa epithelial cells from anti-HIV-1 positive patients

    Journal of Medical Virology, Vol. 77, Núm. 1, pp. 17-22