A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome).
Rump, P.; Niessen, R. C.; Verbruggen, K. T.; Brouwer, O. F.; de Raad, M.; Hordijk, R.; Clinical Genetics, 2011, vol. 79, issue 2, p 183, ISSN 00099163. ISBN 13990004.

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