Publications (36) Publications in which a researcher has participated

1998

  1. 160Thr mutation in the rhodopsin gene associated with retinitis pigmentosa

    Human Heredity, Vol. 48, Núm. 5, pp. 237-240

  2. A c-myc antisense oligonucleotide inhibits human retinal pigment epithelial cell proliferation

    Experimental Eye Research, Vol. 66, Núm. 5, pp. 581-589

  3. A strategy for mt-DNA analysis of hair shafts in practical casework: RE-SSCP.

    PROGRESS IN FORENSIC GENETICS 7

  4. Analisis mutacional del gen PKD1 en pacientes con poliquistosis renal dominante

    Nefrologia, Vol. 18, Núm. 5, pp. 382-388

  5. Aspectos éticos del uso de la prueba de ADN con fines forenses

    Entre el nacer y el morir (Comares), pp. 153-164

  6. Band shift analysis of three base-pair repeat alleles in the short tandem repeat locus D12S391

    Forensic Science International, Vol. 93, Núm. 2-3, pp. 79-88

  7. Bases de datos de ADN con fines de investigación criminal: aspectos técnicos y problemas ético-legales

    Revista de derecho y genoma humano: genética, biotecnología y medicina avanzada, Núm. 8, pp. 137-158

  8. Catalonian population study of the tetranucleotide repeat loci D3S1358, D8S1179, D18S51 and D19S253

    International Journal of Legal Medicine, Vol. 112, Núm. 1, pp. 75-77

  9. Complex STRs (ACTBP2, D21S11 and FIBRA/FGA) in two Spanish populations: New intermediate alleles and population genetic peculiarities in ACTBP2.

    PROGRESS IN FORENSIC GENETICS 7

  10. DNA Recommendations 1997 of the International Society for Forensic Genetics

    Vox Sanguinis

  11. DNA databases for criminal investigation purposes: technical aspects and ethical-legal problems

    Law and the human genome review = Revista de derecho y genoma humano / Chair in Law and the Human Genome, BBV Foundation-Provincial Government of Biscay, University of Deusto, pp. 137-158

  12. Further exploration of new STRs of interest for forensic genetic analysis.

    PROGRESS IN FORENSIC GENETICS 7

  13. Li-Fraumeni syndrome and osteosarcoma of the maxilla

    Journal of Oral and Maxillofacial Surgery, Vol. 56, Núm. 9, pp. 1106-1109

  14. Linkage analysis in a large Spanish family with X-linked retinitis pigmentosa: Phenotype-genotype correlation

    Clinical Genetics, Vol. 54, Núm. 1, pp. 26-32

  15. Low incidence of microsatellite instability in patients with cervical carcinomas

    Diagnostic Molecular Pathology, Vol. 7, Núm. 5, pp. 276-282

  16. MVR analysis of the HRAS1 minisatellite: a new polymorphism of medical, anthropological and forensic interest

    PROGRESS IN FORENSIC GENETICS 7

  17. MVR analysis of the MSY1 minisatellite

    PROGRESS IN FORENSIC GENETICS 7

  18. Manual electrophoretic methods for genotyping amplified STR loci.

    Methods in molecular biology (Clifton, N.J.), Vol. 98, pp. 181-192

  19. Minisatellite variant repeat (MVR) analysis of the HRAS1 minisatellite locus

    Electrophoresis, Vol. 19, Núm. 18, pp. 3084-3089

  20. Natural selection on a vertical environmental gradient in Littorina saxatilis: Analysis of fecundity

    Hydrobiologia, Vol. 378, Núm. 1-3, pp. 89-94