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American Journal of Medical Genetics
|
April 5, 2000
Clinical involvement and protein expression in individuals with the FMR1 premutation
F Tassone, R J Hagerman, A K Taylor, et al.
American Journal of Medical Genetics
|
May 20, 1999
FMRP expression as a potential prognostic indicator in fragile X syndrome
F Tassone, R J Hagerman, D N Iklé, et al.
Genes, Brain, and Behavior
|
December 5, 2013
Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndrome
J-C Yang, C Simon, A Schneider, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2003
Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment
J A Thomas, J Johnson, T L Peterson Kraai, et al.
Brain : a Journal of Neurology
|
July 24, 2002
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
C M Greco, R J Hagerman, F Tassone, et al.
Epilepsia
|
August 17, 1999
Epilepsy and EEG findings in males with fragile X syndrome
S A Musumeci, R J Hagerman, R Ferri, et al.
American Journal of Medical Genetics
|
January 1, 1986
Oral folic acid versus placebo in the treatment of males with the fragile X syndrome
R J Hagerman, A W Jackson, A Levitas, et al.
American Journal of Medical Genetics
|
July 15, 1994
Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing
R J Hagerman, P Wilson, L W Staley, et al.
American Journal of Medical Genetics
|
April 20, 1999
Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report
L J Miller, D N McIntosh, J McGrath, et al.
Neurology
|
July 27, 2005
Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)
D A Hall, E Berry-Kravis, S Jacquemont, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 109) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
April 5, 2000
Clinical involvement and protein expression in individuals with the FMR1 premutation
F Tassone, R J Hagerman, A K Taylor, et al.
American Journal of Medical Genetics
|
May 20, 1999
FMRP expression as a potential prognostic indicator in fragile X syndrome
F Tassone, R J Hagerman, D N Iklé, et al.
Genes, Brain, and Behavior
|
December 5, 2013
Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndrome
J-C Yang, C Simon, A Schneider, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2003
Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment
J A Thomas, J Johnson, T L Peterson Kraai, et al.
Brain : a Journal of Neurology
|
July 24, 2002
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
C M Greco, R J Hagerman, F Tassone, et al.
Epilepsia
|
August 17, 1999
Epilepsy and EEG findings in males with fragile X syndrome
S A Musumeci, R J Hagerman, R Ferri, et al.
American Journal of Medical Genetics
|
January 1, 1986
Oral folic acid versus placebo in the treatment of males with the fragile X syndrome
R J Hagerman, A W Jackson, A Levitas, et al.
American Journal of Medical Genetics
|
July 15, 1994
Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing
R J Hagerman, P Wilson, L W Staley, et al.
American Journal of Medical Genetics
|
April 20, 1999
Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report
L J Miller, D N McIntosh, J McGrath, et al.
Neurology
|
July 27, 2005
Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)
D A Hall, E Berry-Kravis, S Jacquemont, et al.
Page
of 11