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Volumn 6, Issue 2, 2001, Pages 150-159
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Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
a b b b c c d e e f f a g g h a a a a b more.. |
Author keywords
Allelic association; Autism; Cranial circumference; Haplotype relative risk; Linkage disequilibrium; Reeler mouse; Serotonin; Splice junction; Transmission disequilibrium test; Trinucleotide repeat
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Indexed keywords
REELIN;
RNA;
ADOLESCENT;
ADULT;
AGED;
ALLELE;
ARTICLE;
AUTISM;
BRAIN STEM;
CHILD;
CONTROLLED STUDY;
DNA SEQUENCE;
ETHNIC GROUP;
EXON;
FAMILY STUDY;
FEMALE;
GENE;
GENE LINKAGE DISEQUILIBRIUM;
GENE MUTATION;
GENETIC ASSOCIATION;
GENETIC LINKAGE;
GENETIC PREDISPOSITION;
GENOTYPE;
HAPLOTYPE;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
SEROTONIN BLOOD LEVEL;
SOUTHERN BLOTTING;
START CODON;
TRANSCRIPTION REGULATION;
TRINUCLEOTIDE REPEAT;
ADULT;
AGED;
AGED, 80 AND OVER;
ALLELES;
AUTISTIC DISORDER;
BRAIN CHEMISTRY;
CASE-CONTROL STUDIES;
CELL ADHESION MOLECULES, NEURONAL;
EXONS;
EXTRACELLULAR MATRIX PROTEINS;
FAMILY HEALTH;
FEMALE;
GENETIC MARKERS;
GENETIC PREDISPOSITION TO DISEASE;
HAPLOTYPES;
HUMANS;
LINKAGE DISEQUILIBRIUM;
MALE;
MIDDLE AGED;
NERVE TISSUE PROTEINS;
POINT MUTATION;
POLYMORPHISM, SINGLE NUCLEOTIDE;
RISK FACTORS;
RNA SPLICE SITES;
SERINE ENDOPEPTIDASES;
SEROTONIN;
SKULL;
TRINUCLEOTIDE REPEATS;
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EID: 17744393442
PISSN: 13594184
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.mp.4000850 Document Type: Article |
Times cited : (313)
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References (66)
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