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Found 1 from your keywords: author=Peter Hanjo et.al- -
cover
Hair root FMRP expression for screening of fragile X full mutation females
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Lantip RujitoDwi kustianiLies anne severjinenPeter Hanjo et.al- -

The fragile X syndrome is the most common form of inherited mental retardation in humans, caused by an expansion of the cytosine-guanine-guanine (CGG) repeat in the fragile X mental retardation 1 (FMR1) gene located on the X chromosome. Antibody tests have been developed to identify fragile X patients, based on the presence or absence of fragile mental retardation protein (FMRP) in both lymphoc…

Edition
-
ISBN/ISSN
1907-3062
Collation
11p
Series Title
-
Call Number
Universa Medicina, 30 (1) 2011 :11-21