Defining the genetic architecture of human developmental language impairment

Life Sciences

Volumn 90, Issue 13-14, 2012, Pages 469-475

  Li, Ning ^a   Bartlett, Christopher W ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

Association; Dyslexia; Genetic linkage; Language; Reading; Specific language impairment

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); ADENOSINE TRIPHOSPHATASE CALCIUM TRANSPORTING 2C MEMBER 2; BRAIN DERIVED NEUROTROPHIC FACTOR; CONTACTIN; CONTACTIN ASSOCIATION PROTEIN LIKE 2; TRANSCRIPTION FACTOR C MAF; TRANSCRIPTION FACTOR FOXP2; UNCLASSIFIED DRUG;

AUTISM; AUTOPSY; BRAIN; CELLULAR DISTRIBUTION; CHROMOSOME 12; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 19; CHROMOSOME 4; DEVELOPMENTAL DISORDER; GENE INTERACTION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC VARIABILITY; HEREDITY; HUMAN; LANGUAGE; LANGUAGE DISABILITY; MOLECULAR GENETICS; NUCLEAR FAMILY; PEDIGREE; PHENOTYPE; PROTEIN EXPRESSION; REVIEW; SHORT TERM MEMORY; SINGLE NUCLEOTIDE POLYMORPHISM; SPECIFIC LANGUAGE IMPAIRMENT;

ANIMALS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 19; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; LANGUAGE; LANGUAGE DEVELOPMENT DISORDERS; PEDIGREE;

ANIMALIA;

EID: 84863414908     PISSN: 00243205     EISSN: 18790631     Source Type: Journal    
DOI: 10.1016/j.lfs.2012.01.016     Document Type: Review

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