TBR1is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion

A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includesTBR1,TANK, andPSMD14

(2013) Lindsay C. Burrage et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review

(2012) Orazio Palumbo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders

(2012) Sandesh C S Nagamani et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report

(2012) Orazio Palumbo et al.   Molecular Cytogenetics

De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia

(2011) Chiara Magri et al.   European Journal of Medical Genetics

Severe pulmonary emphysema in a girl with interstitial deletion of 2q24.2q24.3 includingITGB6

(2010) Shinichi Takatsuki et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy

(2010) Ana Cristina Victorino Krepischi et al.   EPILEPSIA

The T-box brain 1 (Tbr1) transcription factor inhibits astrocyte formation in the olfactory bulb and regulates neural stem cell fate

(2010) Héctor R. Méndez-Gómez et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

(2010) F. Bedogni et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology

(2009) Francesco Bedogni et al.   GENE EXPRESSION PATTERNS