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E Berry-Kravis

Showing results (31-40 of 38) with videos related to

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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.
Clinical Genetics|July 28, 2015
Neurological and endocrine phenotypes of fragile X carrier womenD Hall, K Todorova-Koteva, S Pandya, et al.
Neurology|January 29, 2003
Apolipoprotein E epsilon4 allele, AD pathology, and the clinical expression of Alzheimer's diseaseD A Bennett, R S Wilson, J A Schneider, 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.
American Journal of Mental Retardation : AJMR|March 6, 2004
Aging in individuals with the FMR1 mutationS Jacquemont, F Farzin, D Hall, et al.
Neurology|December 7, 2007
FMR1 CGG repeat length predicts motor dysfunction in premutation carriersM A Leehey, E Berry-Kravis, C G Goetz, et al.
American Journal of Medical Genetics|January 8, 1999
Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new casesW T Hsu, D A Shchepin, R Mao, et al.
Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
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.
Clinical Genetics|July 28, 2015
Neurological and endocrine phenotypes of fragile X carrier womenD Hall, K Todorova-Koteva, S Pandya, et al.
Neurology|January 29, 2003
Apolipoprotein E epsilon4 allele, AD pathology, and the clinical expression of Alzheimer's diseaseD A Bennett, R S Wilson, J A Schneider, 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.
American Journal of Mental Retardation : AJMR|March 6, 2004
Aging in individuals with the FMR1 mutationS Jacquemont, F Farzin, D Hall, et al.
Neurology|December 7, 2007
FMR1 CGG repeat length predicts motor dysfunction in premutation carriersM A Leehey, E Berry-Kravis, C G Goetz, et al.
American Journal of Medical Genetics|January 8, 1999
Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new casesW T Hsu, D A Shchepin, R Mao, et al.
Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.
Pageof 4