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Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Physical Review Letters|June 25, 2016
Sub-Femto-g Free Fall for Space-Based Gravitational Wave Observatories: LISA Pathfinder ResultsM Armano, H Audley, G Auger, et al.
Translational Medicine @ Unisa|July 31, 2019
The Reference Site Collaborative Network of the European Innovation Partnership on Active and Healthy AgeingJ Bousquet, M Illario, J Farrell, et al.
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