Centro de investigación
Fundación Pública Galega de Medicina Xenómica
Publicacións (36) Publicacións nas que participase algún/ha investigador/a
1998
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160Thr mutation in the rhodopsin gene associated with retinitis pigmentosa
Human Heredity, Vol. 48, Núm. 5, pp. 237-240
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A c-myc antisense oligonucleotide inhibits human retinal pigment epithelial cell proliferation
Experimental Eye Research, Vol. 66, Núm. 5, pp. 581-589
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A strategy for mt-DNA analysis of hair shafts in practical casework: RE-SSCP.
PROGRESS IN FORENSIC GENETICS 7
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Analisis mutacional del gen PKD1 en pacientes con poliquistosis renal dominante
Nefrologia, Vol. 18, Núm. 5, pp. 382-388
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Aspectos éticos del uso de la prueba de ADN con fines forenses
Entre el nacer y el morir (Comares), pp. 153-164
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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
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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
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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
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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
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DNA Recommendations 1997 of the International Society for Forensic Genetics
Vox Sanguinis
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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
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Further exploration of new STRs of interest for forensic genetic analysis.
PROGRESS IN FORENSIC GENETICS 7
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Li-Fraumeni syndrome and osteosarcoma of the maxilla
Journal of Oral and Maxillofacial Surgery, Vol. 56, Núm. 9, pp. 1106-1109
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Linkage analysis in a large Spanish family with X-linked retinitis pigmentosa: Phenotype-genotype correlation
Clinical Genetics, Vol. 54, Núm. 1, pp. 26-32
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Low incidence of microsatellite instability in patients with cervical carcinomas
Diagnostic Molecular Pathology, Vol. 7, Núm. 5, pp. 276-282
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MVR analysis of the HRAS1 minisatellite: a new polymorphism of medical, anthropological and forensic interest
PROGRESS IN FORENSIC GENETICS 7
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MVR analysis of the MSY1 minisatellite
PROGRESS IN FORENSIC GENETICS 7
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Manual electrophoretic methods for genotyping amplified STR loci.
Methods in molecular biology (Clifton, N.J.), Vol. 98, pp. 181-192
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Minisatellite variant repeat (MVR) analysis of the HRAS1 minisatellite locus
Electrophoresis, Vol. 19, Núm. 18, pp. 3084-3089
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Natural selection on a vertical environmental gradient in Littorina saxatilis: Analysis of fecundity
Hydrobiologia, Vol. 378, Núm. 1-3, pp. 89-94