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R J Hagerman

Showing results (31-40 of 109) with videos related to

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Revista De Neurologia|February 27, 2019
[Fragile X associated tremor/ataxia syndrome: its clinical presentation, pathology, and treatment]M J Salcedo-Arellano, R J Hagerman, V Martinez-Cerdeno
Developmental Medicine and Child Neurology|September 30, 1999
Sensory-modulation disruption, electrodermal responses, and functional behaviorsD N McIntosh, L J Miller, V Shyu, et al.
Pediatrics|June 1, 1992
Standards for selected anthropometric measurements in males with the fragile X syndromeM G Butler, A Brunschwig, L K Miller, et al.
American Journal of Medical Genetics|January 1, 1986
Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) femalesM B Kemper, R J Hagerman, R S Ahmad, et al.
Journal of Medical Genetics|July 4, 2001
A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNAF Tassone, R J Hagerman, A K Taylor, et al.
American Journal of Medical Genetics|July 14, 2001
Transcription of the FMR1 gene in individuals with fragile X syndromeF Tassone, R J Hagerman, W D Chamberlain, et al.
American Journal of Medical Genetics|May 20, 1999
Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutationF Tassone, R J Hagerman, L W Gane, et al.
American Journal of Medical Genetics|January 1, 1984
Consideration of connective tissue dysfunction in the fragile X syndromeR J Hagerman, K Van Housen, A C Smith, et al.
American Journal of Medical Genetics|January 1, 1986
Aortic root dilatation and mitral valve prolapse in the fragile X syndromeJ P Loehr, D P Synhorst, R R Wolfe, et al.
Clinical Genetics|September 27, 2012
Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriersY Liu, T I Winarni, L Zhang, et al.
Pageof 11

Showing results (31-40 of 109) with videos related to

Sort By:
Pageof 11
Revista De Neurologia|February 27, 2019
[Fragile X associated tremor/ataxia syndrome: its clinical presentation, pathology, and treatment]M J Salcedo-Arellano, R J Hagerman, V Martinez-Cerdeno
Developmental Medicine and Child Neurology|September 30, 1999
Sensory-modulation disruption, electrodermal responses, and functional behaviorsD N McIntosh, L J Miller, V Shyu, et al.
Pediatrics|June 1, 1992
Standards for selected anthropometric measurements in males with the fragile X syndromeM G Butler, A Brunschwig, L K Miller, et al.
American Journal of Medical Genetics|January 1, 1986
Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) femalesM B Kemper, R J Hagerman, R S Ahmad, et al.
Journal of Medical Genetics|July 4, 2001
A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNAF Tassone, R J Hagerman, A K Taylor, et al.
American Journal of Medical Genetics|July 14, 2001
Transcription of the FMR1 gene in individuals with fragile X syndromeF Tassone, R J Hagerman, W D Chamberlain, et al.
American Journal of Medical Genetics|May 20, 1999
Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutationF Tassone, R J Hagerman, L W Gane, et al.
American Journal of Medical Genetics|January 1, 1984
Consideration of connective tissue dysfunction in the fragile X syndromeR J Hagerman, K Van Housen, A C Smith, et al.
American Journal of Medical Genetics|January 1, 1986
Aortic root dilatation and mitral valve prolapse in the fragile X syndromeJ P Loehr, D P Synhorst, R R Wolfe, et al.
Clinical Genetics|September 27, 2012
Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriersY Liu, T I Winarni, L Zhang, et al.
Pageof 11