Biomedical advances in developmental psychology: the case of fragile X syndrome.

Fragile X syndrome, the most common inherited cause of mental retardation, is caused by an abnormal gene on the bottom end of the X chromosome. Discovered and sequenced in 1991, it is called the Fragile X Mental Retardation-1 (FMR-1) gene. Mutations in the FMR-1 gene include small expansions with...

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Publicado en:Developmental Psychology Vol. 32; pp. 416 - 425
Autor principal: Hagerman, Randi Jenssen
Formato: Artículo
Publicado: American Psychological Association May 1996
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Acceso en línea:Ver este registro en EBSCOhost
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        atl: Biomedical advances in developmental psychology: the case of fragile X syndrome.
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        au: Hagerman, Randi Jenssen
      su:
        Fragile X syndrome
        Behavior genetics
        Genetics
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          Fragile X syndrome
          Behavior genetics
          Genetics
      ab: Fragile X syndrome, the most common inherited cause of mental retardation, is caused by an abnormal gene on the bottom end of the X chromosome. Discovered and sequenced in 1991, it is called the Fragile X Mental Retardation-1 (FMR-1) gene. Mutations in the FMR-1 gene include small expansions with a CGG (a specific sequence of the nucleotides) repetitive sequence that repeats from 50 to 200 times (the premutation) and the full mutation that involves a CGG repeat sequence that is greater than 200. In the full mutation, the FMR-1 gene is usually methylated, turning off the gene so that no protein is produced. Mutations within the FMR-1 gene can cause a spectrum of learning difficulties ranging from mild problems to severe mental retardation. Reprinted by permission of the publisher.
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    language: English
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