Pathogenic Variants In Rlim/Rnf12 Lead To Syndromic X-Linked Intellectual Disability And Congenital, Neurologic And Behavior Disorders
S. G. M. Frints, A. Ozanturk,G. Rodriguez Criado,U. Grasshoff,M. Field,S. Manouvrier-Hanu,S. Hickey,K. Gripp,C. Bauer,C. Schroeder,A. Toutain, T. Mihalic Mosher,B. J. Kelly,P. White,A. Dufke, S. Moon,D. C. Koboldt,E. Gerkes,A. Van Haeringen,C. Ruivenkamp,C. Mignot,B. Keren,A. Mueller,S. Waldmuller, M. Blandfort,U. Kordass, K. Gardner,A. Trimouille,K. E. P. Van Roozendaal,S. A. Haas,L. Murray,E. Haan,R. Carroll,J. Liebelt,L. Hobson,M. De Rademaeker,H. Brunner,J. Glatz,K. Devriendt,J. Vermeesch,M. Raynaud,O. Riess,J. Gribnau,N. Katsanis,P. Bauer,J. Gecz,C. Golzio,C. Gontan,V. Kalscheuer EUROPEAN JOURNAL OF HUMAN GENETICS（2020）
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