Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders-Reference-Cited by-同舟云学术

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Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders

Published:2017-04-13 Issue:6 Volume:173 Page:1649-1655
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Barone Rita¹,Fichera Marco²³,De Grandi Mariaclara¹,Battaglia Marta¹,Lo Faro Valeria²,Mattina Teresa²,Rizzo Renata¹

Affiliation:

1. Department of Clinical and Experimental Medicine, Child Neurology and Psychiatry; University of Catania; Catania Italy

2. Department of Biomedical and Biotechnological Sciences, Medical Genetics; University of Catania; Catania Italy

3. Laboratory of Medical Genetics; I.R.C.C.S. Associazione Oasi Maria Santissima; Troina Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. AutDB: A gene reference resource for autism research;Basu;Nucleic Acids Research,2009

2. Recognizable behavioral and somatic phenotype in patients with proximal interstitial 18q deletion: Report on a new affected child and follow-up on the original reported familial cases;Chudley;American Journal of Medical Genetics Part A,1992

3. The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors;Dougherty;The Journal of Neuroscience,2013

4. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization;Engelen;American Journal of Medical Genetics A,1998

5. Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: An update of the phenotypic map;Feenstra;American Journal of Medical Genetics Part A,2007

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