ListarMED_Articles por tema "Genetics"

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    • openAccess   Gender is a major factor explaining discrepancies in eye colour prediction based on HERC2/OCA2 genotype and the IrisPlex model 

      Martinez-Cadenas, Conrado; Peña Chilet, María; Ibarrola-Villava, Maider; Ribas, Gloria Elsevier (2013)
      In recent years, several studies have greatly increased our understanding of the genetic basis underlying human eye colour variation. A large percentage of the eye colour diversity present in humans can already be genetically ...

    • closedAccess   New insights in primary ciliary dyskinesia 

      Reula, Ana; Moreno-Galdó, Antonio; Romero, Teresa; MILARA, JAVIER; Carda, Carmen; Mata Roig, Manuel; Escribano, Amparo; Dasi, Francisco; Armengot Carceller, Amparo; Lucas, J. S. Taylor & Francis (2017)
      Introduction: Primary ciliary dyskinesia (PCD) is a rare genetic disease with an estimated prevalence of 1:20.000 births. It is characterized by abnormal motility of cilia, leading to impaired mucociliary clearance, and ...