Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates-Reference-Cited by-同舟云学术

Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

Published:2003-04 Issue:4 Volume:72 Page:869-878
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Jacquemont Sébastien,Hagerman Randi J.,Leehey Maureen,Grigsby Jim,Zhang Lin,Brunberg James A.,Greco Claudia,Des Portes Vincent,Jardini Tristan,Levine Richard,Berry-Kravis Elizabeth,Brown W. Ted,Schaeffer Stephane,Kissel John,Tassone Flora,Hagerman Paul J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

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3. Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test;Brown;JAMA,1993

4. Fragile X premutation carriers: characteristic MR imaging findings in adult male patients with progressive cerebellar and cognitive dysfunction;Brunberg;Am J Neurol Radiol,2002

5. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation;Devys;Nat Genet,1993

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