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Genetics / Neurological disorders / Syndromes / Pervasive developmental disorders / Fragile X syndrome / Pediatrics / FMR1 / Chromosomal fragile site / Disability / Health / Medicine / Autism


Fragile X Syndrome First described Martin & Bell (1943): families with sex-linked inheritance for learning difficulties & characteristic physical features. Lubsidentified the chromosome fragile site just above th
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Document Date: 2015-05-13 15:34:38


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City

Newburyport / Baltimore / /

Company

Hatton D.D. / Johns Hopkins University Press / Proc Natl Acad Sci U S A / Paul H. Brookes Publishing Co. / Burns D.D. / /

Country

United States / /

Facility

Hall S.S. / /

IndustryTerm

Treatment of Fragile X Syndrome / fragile site / recurrent otitis media / chromosome fragile site / treatment of adult with fragile X syndrome / /

MedicalCondition

ataxia / premutation disorders / ADHD / neuropathy / autonomic dysfunction / Seizures / echolalia / learning disability / recurrent otitis media / autism / Amygdala dysfunction / intention tremor / joint laxity / mitral valve prolapse / enhanced long term depression / fragile X syndrome / autism spectrum disorder / fragile X-associated tremor ataxia syndrome / flat feet / skin feet / Asperger’s syndrome / white matter disease / strabismus / deficiency / depression / Cluttering / syndrome / disorders / /

Organization

The Johns Hopkins University / FRAXA Research Foundation / /

Person

Randi Hagerman / /

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Position

model for autism and targeted treatments / /

ProvinceOrState

Sussex / California / Massachusetts / /

Technology

gene expression / MRI / /

SocialTag