Loss-of-Function Mutations inEuchromatin Histone Methyl Transferase 1(EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome


Tjitske Kleefstra,Han G. Brunner,Jeanne Amiel,Astrid R. Oudakker,Willy M. Nillesen,Alex Magee,David Geneviève,Valérie Cormier-Daire,Hilde van Esch,Jean-Pierre Fryns,Ben C.J. Hamel,Erik A. Sistermans,Bert B.A. de Vries,Hans van Bokhoven


The American Journal of Human Genetics




August 2006

Copyright © 2006, Elsevier

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