Fundación Pública Galega de Medicina Xenómica

2005

1. A collaborative study of the EDNAP group regarding Y-chromosome binary polymorphism analysis

   Forensic Science International, Vol. 153, Núm. 2-3, pp. 103-108

2. A critical reassessment of the role of mitochondria in tumorigenesis

   PLoS Medicine, Vol. 2, Núm. 11, pp. 1158-1166

3. A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics

   Biochemical and Biophysical Research Communications, Vol. 335, Núm. 3, pp. 891-899

4. Autosomic STR population data in two Caribbean samples from Colombia

   Forensic Science International, Vol. 152, Núm. 1, pp. 79-81

5. Charting the ancestry of African Americans

   American Journal of Human Genetics, Vol. 77, Núm. 4, pp. 676-680

6. Cognitive profile in Williams syndrome: A case study

   British Journal of Developmental Disabilities, Vol. 51, Núm. 2, pp. 143-153

7. Cáncer de mama y ovario hereditario: consejo genético, seguimiento y reducción del riesgo

   Psicooncología: investigación y clínica biopsicosocial en oncología, Vol. 2, Núm. 2, pp. 229-242

8. El decúbito prono en una unidad de cuidados críticos: protocolo y plan de cuidados. Primera parte

   Nursing, Vol. 23, Núm. 6, pp. 56

9. El decúbito prono en una unidad de cuidados críticos: protocolo y plan de cuidados. Segunda parte

   Nursing, Vol. 23, Núm. 7, pp. 56

10. Forensic DNA-typing technologies: a review.

    Methods in molecular biology (Clifton, N.J.), Vol. 297, pp. 1-12

11. Gene expression profile in oral squamous cell carcinoma: A pilot study

    Journal of Oral and Maxillofacial Surgery, Vol. 63, Núm. 6, pp. 786-792

12. Genotyping SNPs with the LightCycler.

    Methods in molecular biology (Clifton, N.J.), Vol. 297, pp. 127-140

13. Hierarchical analysis of 30 Y-chromosome SNPs in European populations

    International Journal of Legal Medicine, Vol. 119, Núm. 1, pp. 10-15

14. Human genome-wide screen of haplotype-like blocks of reduced diversity

    Gene, Vol. 349, pp. 219-225

15. Introduction of an single nucleotide polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

    Electrophoresis, Vol. 26, Núm. 23, pp. 4411-4420

16. Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein

    Journal of Pediatric Endocrinology and Metabolism, Vol. 18, Núm. 6, pp. 545-548

17. Mutation rates at Y chromosome specific microsatellites

    Human Mutation, Vol. 26, Núm. 6, pp. 520-528

18. Neurogenic arthogryposis multiplex congenita and velopharyngeal incompetence associated with chromosome 22q11.2 deletion

    Journal of Child Neurology, Vol. 20, Núm. 1, pp. 76-78

19. PLGA:poloxamer and PLGA:poloxamine blend nanoparticles: New carriers for gene delivery

    Biomacromolecules, Vol. 6, Núm. 1, pp. 271-278

20. Relative efficiency of the linkage disequilibrium mapping approach in detecting candidate genes for schizophrenia in different european populations

    Genomics, Vol. 86, Núm. 3, pp. 280-286