Genetic insights into the functional elements of language

Human Genetics

Volumn 132, Issue 9, 2013, Pages 959-986

  Szalontai, Adam ^a   Csiszar, Katalin ^b  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^b UNIVERSITY OF HAWAII   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATASE; METHYL CPG BINDING PROTEIN 2; NEUREXIN; NEUROLIGIN; TRANSCRIPTION FACTOR FOXP2;

APRAXIA; APRAXIA OF SPEECH; AUTISM; BRAIN FUNCTION; BRAIN GROWTH; CEREBELLUM; CHROMOSOME 22; CHROMOSOME 4P; CHROMOSOME DELETION; COGNITION; COGNITIVE DEFECT; CORPUS CALLOSUM; DEVELOPMENTAL STAGE; DISEASES; ENVIRONMENTAL FACTOR; EPILEPSY; EPILEPTIC DISCHARGE; EXECUTIVE FUNCTION; FRAGILE X SYNDROME; GENE DELETION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HAPPY PUPPET SYNDROME; HUMAN; HYPOPLASIA; INFERIOR FRONTAL GYRUS; KLINEFELTER SYNDROME; LANGUAGE; LANGUAGE ABILITY; LANGUAGE DELAY; LANGUAGE DEVELOPMENT; LANGUAGE DISABILITY; LANGUAGE PROCESSING; LEARNING DISORDER; LEFT HEMISPHERE; MACROCEPHALY; MENTAL DEFICIENCY; MICROCEPHALY; MIDDLE TEMPORAL GYRUS; MISSENSE MUTATION; MOTOR COORDINATION; MOTOR DEVELOPMENT; MOTOR DYSFUNCTION; NERVE CELL; NERVE CELL DIFFERENTIATION; NERVE CELL NETWORK; NERVE CELL PLASTICITY; NERVE FIBER GROWTH; NERVOUS SYSTEM DEVELOPMENT; NOONAN SYNDROME; PHENOTYPE; POSTNATAL GROWTH; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETT SYNDROME; REVIEW; SHORT TERM MEMORY; SIGNAL TRANSDUCTION; SPEECH AND LANGUAGE; SPEECH DELAY; SPEECH DEVELOPMENT; SPEECH DISORDER; STUTTERING; WHITE MATTER; WILLIAMS BEUREN SYNDROME; WOLF HIRSCHHORN SYNDROME; X CHROMOSOME; Y CHROMOSOME;

GENE REGULATORY NETWORKS; GENETIC ASSOCIATION STUDIES; HUMANS; LANGUAGE DEVELOPMENT; LANGUAGE DISORDERS; PHENOTYPE; SIGNAL TRANSDUCTION; SPEECH DISORDERS;

EID: 84882605262     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-013-1317-0     Document Type: Review

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