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American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 114, Issue 5, 2002, Pages 566-569

Evaluation of FOXP2 as an autism susceptibility gene

(7) Wassink, Thomas H a Piven, Joseph b Vieland, Veronica J a,c Pietila, Jennifer a Goedken, Rhinda J c Folstein, Susan E d Sheffield, Val C a

a UNIVERSITY OF IOWA (United States)

b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE (United States)

c UNIVERSITY OF IOWA (United States)

d TUFTS UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

Chromosome 7; Forkhead; Linkage; Linkage disequilibrium; Specific language impairment

Indexed keywords

ALLELE; ARTICLE; AUTISM; EXON; FAMILY STUDY; GENE; GENE FOXP2; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENE SEQUENCE; GENE TECHNOLOGY; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SPEECH DISORDER;

ALLELES; AUTISTIC DISORDER; BASE SEQUENCE; DNA; DNA MUTATIONAL ANALYSIS; FAMILY; FAMILY HEALTH; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MICROSATELLITE REPEATS; PEPTIDES; PHENOTYPE; POLYMORPHISM, GENETIC; REPRESSOR PROTEINS; SEQUENCE DELETION; TRANSCRIPTION FACTORS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0037043075 PISSN: 15524841 EISSN: 1552485X Source Type: Journal
DOI: 10.1002/ajmg.10415 Document Type: Article

Times cited : (68)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.