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Volumn 7, Issue 7, 2002, Pages 801-804
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Absence of association between a polymorphic GGC repeat in the 5’ untranslated region of the reelin gene and autism
a a a a b a,c c d d d e f f f g h i j j j more.. |
Author keywords
Association study; Autistic disorder; Neurodevelopment; Reelin; Transmission disequilibrium test
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Indexed keywords
CYTOSINE;
GUANINE;
NUCLEOTIDE;
REELIN;
5' UNTRANSLATED REGION;
ARTICLE;
AUTISM;
CHILD;
CONTROLLED STUDY;
FAMILY STUDY;
FEMALE;
GENE LINKAGE DISEQUILIBRIUM;
GENETIC ASSOCIATION;
GENETIC HETEROGENEITY;
GENETIC POLYMORPHISM;
GENETIC RISK;
GENETIC SUSCEPTIBILITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
RISK FACTOR;
TRINUCLEOTIDE REPEAT;
5' UNTRANSLATED REGIONS;
AUTISTIC DISORDER;
CELL ADHESION MOLECULES, NEURONAL;
EXTRACELLULAR MATRIX PROTEINS;
FAMILY HEALTH;
FEMALE;
GENOTYPE;
HUMANS;
LINKAGE DISEQUILIBRIUM;
MALE;
NERVE TISSUE PROTEINS;
SERINE ENDOPEPTIDASES;
TRINUCLEOTIDE REPEATS;
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EID: 0036365647
PISSN: 13594184
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.mp.4001071 Document Type: Article |
Times cited : (92)
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References (30)
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