Publicacións nas que colabora con María José Brión Martínez (6)

2014

  1. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    Nature Genetics, Vol. 46, Núm. 8, pp. 826-836

2010

  1. A new approach to long QT syndrome mutation detection by Sequenom MassARRAY® system

    Electrophoresis, Vol. 31, Núm. 10, pp. 1648-1655

  2. Identification of a novel mutation in the human PDE6A gene in autosomal recessive retinitis pigmentosa: Homology with the nmf28/nmf28 mice model

    Clinical Genetics

  3. LARGE-SCALE MUTATION SCREENING IN SUDDEN CARDIAC DEATH (SCD)

    ACTA MEDICINAE LEGALIS ET SOCIALIS (UNIV COIMBRA), pp. 211-217

  4. New technologies in the genetic approach to sudden cardiac death in the young

    Forensic Science International, Vol. 203, Núm. 1-3, pp. 15-24

2003

  1. Typing Y-chromosome single nucleotide polymorphisms with DNA microarray technology

    International Congress Series, Vol. 1239, Núm. C, pp. 21-25