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

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

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

(2011) Anne Gregor et al.   BMC Medical Genetics

Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment

(2011) C. Palka et al.   PEDIATRICS

An extended Family with a Dominantly Inherited Speech Disorder

(2010) J. A. Hurst et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex

(2010) Patrice Roll et al.   HUMAN MOLECULAR GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Language Features in a Mother and Daughter of a Chromosome 7;13 Translocation Involving FOXP2

(2009) J. Bruce Tomblin et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH

A Nonword Repetition Task for Speakers With Misarticulations: The Syllable Repetition Task (SRT)

(2009) Lawrence D. Shriberg et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH