Behavior of 10 patients with FG syndrome (Opitz–Kaveggia syndrome) and the p.R961W mutation in the MED12 gene

J. Graham,J. Visootsak,E. Dykens,Lillie Huddleston,R. Clark,K. L. Jones,J. Moeschler,J. Opitz,Jackie Morford,R. Simensen,R. C. Rogers,C. Schwartz,M. Friez,R. Stevenson

Published 2008 in American Journal of Medical Genetics. Part A

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