Search Results - "Staley, Louise W"

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  1. 1

    Learning-disabled males with a fragile X CGG expansion in the upper premutation size range by HAGERMAN, R. J, STALEY, L. W, O'CONNER, R, LUGENBEEL, K, MCLEAN, S. D, TAYLOR, A

    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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  2. 2

    Molecular Predictors of Cognitive Involvement in Female Carriers of Fragile X Syndrome by Taylor, Annette K, Safanda, John F, Fall, Majilinde Z, Quince, Cindy, Lang, Kirsten A, Hull, Claire E, Carpenter, Isabelle, Staley, Louise W, Hagerman, Randi J

    “…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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  3. 3

    Molecular-clinical correlations in children and adults with fragile X syndrome by Staley, L W, Hull, C E, Mazzocco, M M, Thibodeau, S N, Snow, K, Wilson, V L, Taylor, A, McGavran, L, Weiner, D, Riddle, J

    “…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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  4. 4

    High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression by Hagerman, R J, Hull, C E, Safanda, J F, Carpenter, I, Staley, L W, O'Connor, R A, Seydel, C, Mazzocco, M M, Snow, K, Thibodeau, S N

    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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  5. 5

    Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing by Hagerman, R J, Wilson, P, Staley, L W, Lang, K A, Fan, T, Uhlhorn, C, Jewell-Smart, S, Hull, C, Drisko, J, Flom, K

    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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