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Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.

Am J Hum Genet, Vol. 79, No. 2. (August 2006), pp. 370-377.

by T. Kleefstra, H. G. Brunner, J. Amiel, et al.A. R. Oudakker, W. M. Nillesen, A. Magee, D. Geneviève, V. Cormier-Daire, H. van Esch, J. P. Fryns, B. C. Hamel, E. A. Sistermans, B. B. de Vries, H. van Bokhoven

posted to 9q43 ehmt1 jouberts-syndrome mir by dchughes on 2006-11-29 10:38:44 as

along with 2 groups G4ID Genetics-of-Gambling

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