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Medicina (B.Aires) ; 55(5/1): 457-66, 1995. graf
Article in Spanish | LILACS | ID: lil-161623

ABSTRACT

The Fragile X syndrome is one of the most frequent forms of mental retardation. The responsible mutation is an unstable repetitive sequence. Since the mutation's discovery, the knowledge about the gene, its protein, function, expression, laboratory detection, phenotype-genotype relationship and risk of expansion, has enormously increased. This work pretends to review the recent advances in this syndrome in all its aspects.


Subject(s)
Humans , Male , Female , Fragile X Syndrome/genetics , CpG Islands/genetics , DNA , Gene Expression Regulation , Genotype , Methylation , Mutation , Phenotype , Nerve Tissue Proteins/physiology , Risk Factors , Repetitive Sequences, Nucleic Acid , Fragile X Syndrome/diagnosis
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