A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism

A novel X-linked disorder with developmental delay and autistic features

(2011) Namik Kaya et al.   ANNALS OF NEUROLOGY

Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12 → q13.3) inherited from the mother

(2010) C. Apacik et al.   CLINICAL GENETICS

Inherited tandem duplication dup(X) (q131-q212) in a male proband

(2010) Lars O. Vejerslev et al.   CLINICAL GENETICS

AUTISM SPECTRUM DISORDERS IN CHILDREN WITH PHYSICAL OR MENTAL DISABILITY OR BOTH. I: CLINICAL AND EPIDEMIOLOGICAL ASPECTS

(2010) Viviann Nordin et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome

(2010) W. Edward Visser et al.   HUMAN MOLECULAR GENETICS

Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax

(2009) Dorien Lugtenberg et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A synaptic trek to autism

(2009) Thomas Bourgeron   CURRENT OPINION IN NEUROBIOLOGY