Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndrome-Reference-Cited by-同舟云学术

Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndrome

Published:2006 Issue:6 Volume:140A Page:618-623
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kleefstra Tjitske,Koolen David A.,Nillesen Willy M.,de Leeuw Nicole,Hamel Ben C.J.,Veltman Joris A.,Sistermans Erik A.,van Bokhoven Hans,van Ravenswaay Conny,de Vries Bert B.A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Syndromes of disordered chromatin remodeling

2. A report of a child with a deletion (9)(q34.3): a recognisable phenotype?

3. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements

4. Aplasia cutis congenita with chromosome 12q abnormality.

5. Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome

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