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R J Hagerman

Showing results (91-100 of 109) with videos related to

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JAMA|February 16, 1994
Molecular predictors of cognitive involvement in female carriers of fragile X syndromeA K Taylor, J F Safanda, M Z Fall, et al.
Genes, Brain, and Behavior|January 25, 2012
Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndromeC A Hoeffer, E Sanchez, R J Hagerman, et al.
Brain : a Journal of Neurology|October 26, 2005
Protein composition of the intranuclear inclusions of FXTASC K Iwahashi, D H Yasui, H-J An, et al.
American Journal of Medical Genetics|July 15, 1994
High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expressionR J Hagerman, C E Hull, J F Safanda, et al.
Clinical Genetics|January 17, 2014
Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansionD Z Loesch, M Q Bui, E Hammersley, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|November 1, 1994
Fragile X syndrome in a normal IQ male with learning and emotional problemsS A Merenstein, V Shyu, W E Sobesky, et al.
Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.
American Journal of Medical Genetics|December 18, 1995
Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolismM B Schapiro, D G Murphy, R J Hagerman, et al.
American Journal of Medical Genetics|July 9, 1999
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal developmentD L Freedenberg, L W Gane, C S Richards, et al.
American Journal of Mental Retardation : AJMR|March 6, 2004
Aging in individuals with the FMR1 mutationS Jacquemont, F Farzin, D Hall, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
JAMA|February 16, 1994
Molecular predictors of cognitive involvement in female carriers of fragile X syndromeA K Taylor, J F Safanda, M Z Fall, et al.
Genes, Brain, and Behavior|January 25, 2012
Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndromeC A Hoeffer, E Sanchez, R J Hagerman, et al.
Brain : a Journal of Neurology|October 26, 2005
Protein composition of the intranuclear inclusions of FXTASC K Iwahashi, D H Yasui, H-J An, et al.
American Journal of Medical Genetics|July 15, 1994
High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expressionR J Hagerman, C E Hull, J F Safanda, et al.
Clinical Genetics|January 17, 2014
Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansionD Z Loesch, M Q Bui, E Hammersley, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|November 1, 1994
Fragile X syndrome in a normal IQ male with learning and emotional problemsS A Merenstein, V Shyu, W E Sobesky, et al.
Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.
American Journal of Medical Genetics|December 18, 1995
Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolismM B Schapiro, D G Murphy, R J Hagerman, et al.
American Journal of Medical Genetics|July 9, 1999
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal developmentD L Freedenberg, L W Gane, C S Richards, et al.
American Journal of Mental Retardation : AJMR|March 6, 2004
Aging in individuals with the FMR1 mutationS Jacquemont, F Farzin, D Hall, et al.
Pageof 11