"Resumen: Este trabajo es una réplica al artículo de Joseba Lakarra (2010), publicado en Veleia 27. Se intenta aquí demostrar que no existe incompatibilidad entre los numerales ibéricos propuestos en Orduña (2005) y Ferrer i Jané (2009) y…
We performed a comprehensive assessment of rare inherited variation in autism spectrum disorder (ASD) by analyzing whole-genome sequences of 2,308 individuals from families with multiple affected children.
Dies betrifft unter anderem alle Mannschaften der englischen Premier League und die meisten Mannschaften der spanischen Primera División und der italienischen Serie A. Diese tauchen daher in dieser Liste nicht auf, obwohl die…
CUL4A and B encode subunits of E3-ubiquitin ligases implicated in diverse processes including nucleotide excision repair, regulating gene expression and controlling DNA replication fork licensing.
Hereditary hypertrichoses are a group of hair overgrowth syndromes that are extremely rare in humans. We have previously demonstrated that a position effect on TRPS1 is associated with hypertrichosis in humans and mice.
Human fibrinogen1,2 is produced in the liver from three homologous polypeptide chains, Bβ, Aa and g encoded by the fibrinogen gene cluster FGB, FGA and FGG, on human chromosome 4. Two copies of each polypeptide chain assemble to form a…