Related references
Note: Only part of the references are listed.Maternally and Paternally Inherited Deletion of 7q31 Involving the FOXP2 Gene in Two Families
O. Zilina et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
Phenotype of FOXP2 Haploinsufficiency in a Mother and Son
Gregory M. Rice et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment
Chiara Palka et al.
PEDIATRICS (2012)
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
Anne Gregor et al.
BMC MEDICAL GENETICS (2011)
An extended Family with a Dominantly Inherited Speech Disorder
J. A. Hurst et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
Patrice Roll et al.
HUMAN MOLECULAR GENETICS (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
Prateek Kumar et al.
NATURE PROTOCOLS (2009)
Language Features in a Mother and Daughter of a Chromosome 7;13 Translocation Involving FOXP2
J. Bruce Tomblin et al.
JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH (2009)
A Nonword Repetition Task for Speakers With Misarticulations: The Syllable Repetition Task (SRT)
Lawrence D. Shriberg et al.
JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH (2009)
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
Sonja C. Vernes et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain
Elizabeth Spiteri et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Deletion of 7q31-1 supports involvement of FOXP2 in language impairment:: Clinical report and review
P. A. Lennon et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
Lars Feuk et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2
Lawrence D. Shriberg et al.
JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH (2006)
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
S Zeesman et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
KD MacDermot et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
FOXP2 and the neuroanatomy of speech and language
F Vargha-Khadem et al.
NATURE REVIEWS NEUROSCIENCE (2005)
A forkhead-domain gene is mutated in a severe speech and language disorder
CSL Lai et al.
NATURE (2001)
Oral dyspraxia in inherited speech and language impairment and acquired dysphasia
KJ Alcock et al.
BRAIN AND LANGUAGE (2000)