Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome-Reference-Cited by-同舟云学术

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

Published:2006-08 Issue:2 Volume:79 Page:370-377
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference28 articles.

1. Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation;Harada;J Med Genet,2004

2. A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome;Harada;J Hum Genet,2004

3. 9q34.3 Deletion syndrome in three unrelated children;Iwakoshi;Am J Med Genet A,2004

4. Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome;Stewart;Am J Med Genet A,2004

5. Three patients with terminal deletions within the subtelomeric region of chromosome 9q;Neas;Am J Med Genet A,2005

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