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Volumn 74, Issue 4, 1997, Pages 453-454
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Polymorphism of FXR1 showing lack of association with autism.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
FXR1 PROTEIN, HUMAN;
RNA BINDING PROTEIN;
AUTISM;
CHROMOSOME 3;
COMPARATIVE STUDY;
FRAGILE X SYNDROME;
GENETIC SCREENING;
GENETICS;
GENOTYPE;
HUMAN;
LETTER;
NUCLEOTIDE SEQUENCE;
PSYCHOLOGICAL ASPECT;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
AUTISTIC DISORDER;
CHROMOSOMES, HUMAN, PAIR 3;
DNA MUTATIONAL ANALYSIS;
FRAGILE X SYNDROME;
GENETIC SCREENING;
GENOTYPE;
HUMANS;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
RNA-BINDING PROTEINS;
MLCS;
MLOWN;
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EID: 0031586148
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/(sici)1096-8628(19970725)74:4<453::aid-ajmg21>3.3.co;2-z Document Type: Letter |
Times cited : (6)
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References (0)
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