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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 behaviors
D N McIntosh, L J Miller, V Shyu, et al.
Pediatrics
|
June 1, 1992
Standards for selected anthropometric measurements in males with the fragile X syndrome
M 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) females
M 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 RNA
F 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 syndrome
F 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 premutation
F 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 syndrome
R 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 syndrome
J 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 carriers
Y Liu, T I Winarni, L Zhang, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 109) with videos related to
Sort By:
Page
of 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 behaviors
D N McIntosh, L J Miller, V Shyu, et al.
Pediatrics
|
June 1, 1992
Standards for selected anthropometric measurements in males with the fragile X syndrome
M 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) females
M 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 RNA
F 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 syndrome
F 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 premutation
F 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 syndrome
R 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 syndrome
J 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 carriers
Y Liu, T I Winarni, L Zhang, et al.
Page
of 11