Related references
Note: Only part of the references are listed.Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment
Chiara Palka et al.
PEDIATRICS (2012)
Genetics of Speech and Language Disorders
Changsoo Kang et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 12 (2011)
Rab6, Rab8, and MICAL3 Cooperate in Controlling Docking and Fusion of Exocytotic Carriers
Ilya Grigoriev et al.
CURRENT BIOLOGY (2011)
1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay
Ahmed T. Abdelmoity et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2011)
SynArfGEF is a guanine nucleotide exchange factor for Arf6 and localizes preferentially at post-synaptic specializations of inhibitory synapses
Masahiro Fukaya et al.
JOURNAL OF NEUROCHEMISTRY (2011)
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
Brian J. O'Roak et al.
NATURE GENETICS (2011)
The Hypothesis of Apraxia of Speech in Children with Autism Spectrum Disorder
Lawrence D. Shriberg et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2011)
De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
Fadi F. Hamdan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Delineation of 15q13.3 microdeletions
A. Masurel-Paulet et al.
CLINICAL GENETICS (2010)
Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency
Christopher W. Carr et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
CAST and ELKS proteins: structural and functional determinants of the presynaptic active zone
Yamato Hida et al.
JOURNAL OF BIOCHEMISTRY (2010)
Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients
Ester Saus et al.
JOURNAL OF PSYCHIATRIC RESEARCH (2010)
The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia
E. K. Green et al.
MOLECULAR PSYCHIATRY (2010)
Which Neurodevelopmental Disorders Get Researched and Why?
Dorothy V. M. Bishop
PLOS ONE (2010)
2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene
Caroline Rooryck et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2009)
A 785 kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
Mitchel J. Pariani et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2009)
FOXP2 as a molecular window into speech and language
Simon E. Fisher et al.
TRENDS IN GENETICS (2009)
A Functional Genetic Link between Distinct Developmental Language Disorders
Sonja C. Vernes et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Subtelomeric imbalances in phenotypically normal individuals
Irina Balikova et al.
HUMAN MUTATION (2007)
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
Lars Feuk et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Subtelomere FISH analysis of 11 688 cases: An evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities
J. B. Ravnan et al.
JOURNAL OF MEDICAL 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)
SRPX2 mutations in disorders of language cortex and cognition
P Roll et al.
HUMAN MOLECULAR GENETICS (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)
The prevalence of autistic spectrum disorders in adolescents with a history of specific language impairment (SLI)
Gina Conti-Ramsden et al.
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2006)
Genetic influences on language impairment and phonological short-term memory
DF Newbury et al.
TRENDS IN COGNITIVE SCIENCES (2005)
ELKS, a protein structurally related to the active zoneassociated protein CAST, is expressed in pancreatic β cells and functions in insulin exocytosis:: Interaction of ELKS with exocytotic machinery analyzed by total internal reflection fluorescence microsscopy
M Ohara-Imaizumi et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
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)
Diagnostic criteria of developmental apraxia of speech used by clinical speech-language pathologists
K Forrest
AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY (2003)
A familial cryptic subtelomeric deletion 12p with variable phenotypic effect
E Baker et al.
CLINICAL GENETICS (2002)
A forkhead-domain gene is mutated in a severe speech and language disorder
CSL Lai et al.
NATURE (2001)
Share Paper
