Cognitive-behavioral characteristics and developmental trajectories in children with deletion 11qter (Jacobsen syndrome), and their relation to deletion size-Reference-Cited by-同舟云学术

Cognitive-behavioral characteristics and developmental trajectories in children with deletion 11qter (Jacobsen syndrome), and their relation to deletion size

Published:2014-11-25 Issue:1 Volume:167 Page:45-53
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fisch Gene S.¹

Affiliation:

1. Department of Epidemiology & Health Promotion; New York University Colleges of Dentistry and Nursing; New York City New York

Funder

LeJeune Fondation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36837/fullpdf

Reference35 articles.

1. Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability;Bhalla;Am J Hum Genet,2008

2. Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion;Böhm;Am J Med Genet A,2006

3. Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome);Coldren;Neurogenetics,2009

4. Two children with subtelomeric 11q deletions: A description and interpretation of their clinical presentations and molecular genetic findings;Cox;Clin Dysmorphol,2009

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2. Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size;American Journal of Medical Genetics Part A;2016-06-09