Phenotype of FOXP2 haploinsufficiency in a mother and son

Human I-mfa domain proteins specifically interact with KSHV LANA and affect its regulation of Wnt signaling-dependent transcription

(2010) Shuichi Kusano et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Genetic Advances in the Study of Speech and Language Disorders

(2010) D.F. Newbury et al.   NEURON

Extensions to the Speech Disorders Classification System (SDCS)

(2010) Lawrence D. Shriberg et al.   CLINICAL LINGUISTICS & PHONETICS

Prevalence and Phenotype of Childhood Apraxia of Speech in Youth With Galactosemia

(2010) Lawrence D. Shriberg et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH

Unravelling neurogenetic networks implicated in developmental language disorders

(2009) Sonja C. Vernes et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Associations of postural knowledge and basic motor skill with dyspraxia in autism: Implication for abnormalities in distributed connectivity and motor learning.

(2009) Lauren R. Dowell et al.   NEUROPSYCHOLOGY

FOXP2 as a molecular window into speech and language

(2009) Simon E. Fisher et al.   TRENDS IN GENETICS

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

Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS)

(2008) Lawrence D. Shriberg et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits

(2008) Matthias Groszer et al.   CURRENT BIOLOGY

The Genetics of Speech and Language Impairments

(2008) Karin Stromswold   NEW ENGLAND JOURNAL OF MEDICINE

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE