Skip to main content

and
Your search also matched 1 preview-only Content is preview-only when you or your institution have not yet subscribed to it.

By making our abstracts and previews universally accessible we help you purchase only the content that is relevant to you.
results, e.g.

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young

Include preview-only content
  1. Article

    Open Access

    3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome

    Roberts syndrome (RBS) is a rare autosomal recessive disorder mainly characterized by growth retardation, limb defects and craniofacial anomalies. Characteristic cytogenetic findings are "railroad track" appea...

    Celine Dupont, Martine Bucourt, Fabien Guimiot, Lilia Kraoua in Molecular Cytogenetics (2014)