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

Author:

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

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

August 2006

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