Researchers from UCL (University College London) and the ESRF (The European Synchrotron) have produced the first ...
Researchers have identified bi-allelic variants in the POPDC2 gene as the cause of a rare inherited cardiac syndrome characterized by sinus node dysfunction, atrioventricular (AV) conduction defects ...
“For more than a century, radiology and histology have offered very different views of the body. The HiP-CT synchrotron ...
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