Search Results - "Staley, Louise W"
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Learning-disabled males with a fragile X CGG expansion in the upper premutation size range
Published in Pediatrics (Evanston) (1996)“…There is a broad spectrum of clinical involvement in both boys and girls affected by fragile X syndrome. Although this disorder is best known as the most…”
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Molecular Predictors of Cognitive Involvement in Female Carriers of Fragile X Syndrome
Published in JAMA : the journal of the American Medical Association (16-02-1994)“…Objective.—Fragile X syndrome is caused by a mutation involving expansion of a CGG trinucleotide repeat segment in the fragile X mental retardation—1 (FMR1)…”
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Molecular-clinical correlations in children and adults with fragile X syndrome
Published in American journal of diseases of children (1960) (01-07-1993)“…Fragile X syndrome is the most commonly known inherited form of mental retardation. The intellectual abilities range from a normal IQ with learning…”
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High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression
Published in American journal of medical genetics (15-07-1994)“…Fragile X (fra(X)) males with a standardized IQ score of 70 or higher represent a high functioning (HF) or nonretarded fra(X) male group. This group, which…”
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Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing
Published in American journal of medical genetics (15-07-1994)“…We describe a pilot project utilizing saliva to identify the FMR-1 mutation in high-risk special education students from four public school districts in…”
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