A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2

(2015) Daniela Moralli et al.   Molecular Cytogenetics

Transcriptional enhancers: from properties to genome-wide predictions

(2014) Daria Shlyueva et al.   NATURE REVIEWS GENETICS

De novo TBR1 mutations in sporadic autism disrupt protein functions

(2014) Pelagia Deriziotis et al.   Nature Communications

Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

(2013) Samantha J Turner et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization

(2012) Jennifer J.S. Laffin et al.   GENETICS IN MEDICINE

An integrated encyclopedia of DNA elements in the human genome

(2012)   NATURE

Topological domains in mammalian genomes identified by analysis of chromatin interactions

(2012) Jesse R. Dixon et al.   NATURE

Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development

(2012) Stefan Bonn et al.   NATURE GENETICS

Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families

(2011) O. Žilina et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Phenotype of FOXP2 haploinsufficiency in a mother and son

(2011) Gregory M. Rice et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment

(2011) C. Palka et al.   PEDIATRICS

Predictive chromatin signatures in the mammalian genome

(2009) G. C. Hon et al.   HUMAN MOLECULAR GENETICS

Multiple transcription start sites for FOXP2 with varying cellular specificities

(2008) Diane I. Schroeder et al.   GENE