Interstitial microdeletions including the chromosome band 4q13.2 and theUBA6gene as possible causes of intellectual disability and behavior disorder

Impairment of social behavior and communication in mice lacking the Uba6-dependent ubiquitin activation system

(2015) Ji Yeon Lee et al.   BEHAVIOURAL BRAIN RESEARCH

4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence ofKIThaploinsufficiency

(2014) Parisa Hemati et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Etiological yield of SNP microarrays in idiopathic intellectual disability

(2014) G. Eda Utine et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Insertional translocation leading to a 4q13 duplication including theEPHA5gene in two siblings with attention-deficit hyperactivity disorder

(2013) Eunice Matoso et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Microdeletions of 5.5 Mb (4q13.2-q13.3) and 4.1 Mb (7p15.3-p21.1) associated with a saethre-chotzen-like phenotype, severe intellectual disability, and autism

(2013) Shino Shimada et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Global increases in both common and rare copy number load associated with autism

(2013) Santhosh Girirajan et al.   HUMAN MOLECULAR GENETICS

Altered Social Behavior and Neuronal Development in Mice Lacking the Uba6-Use1 Ubiquitin Transfer System

(2013) Peter C.W. Lee et al.   MOLECULAR CELL

A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability

(2012) Anunchai Assawamakin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE