Search research articles
Contact Us
Filters
Showing results (91-100 of 109) with videos related to
Page
of 11
Sort By:
JAMA
|
February 16, 1994
Molecular predictors of cognitive involvement in female carriers of fragile X syndrome
A 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 syndrome
C A Hoeffer, E Sanchez, R J Hagerman, et al.
Brain : a Journal of Neurology
|
October 26, 2005
Protein composition of the intranuclear inclusions of FXTAS
C 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 expression
R 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 expansion
D 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 problems
S A Merenstein, V Shyu, W E Sobesky, et al.
Clinical Genetics
|
May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia
T 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 metabolism
M 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 development
D 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 mutation
S Jacquemont, F Farzin, D Hall, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 109) with videos related to
Sort By:
Page
of 11
JAMA
|
February 16, 1994
Molecular predictors of cognitive involvement in female carriers of fragile X syndrome
A 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 syndrome
C A Hoeffer, E Sanchez, R J Hagerman, et al.
Brain : a Journal of Neurology
|
October 26, 2005
Protein composition of the intranuclear inclusions of FXTAS
C 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 expression
R 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 expansion
D 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 problems
S A Merenstein, V Shyu, W E Sobesky, et al.
Clinical Genetics
|
May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia
T 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 metabolism
M 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 development
D 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 mutation
S Jacquemont, F Farzin, D Hall, et al.
Page
of 11