Grasso, Marina <br/><br/>
The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype.  [electronic resource] 

 -  Molecular and cellular probes  Apr 2010 
 - 107-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-1194 
<br/><br/><label>Standard No.: </label>10.1016/j.mcp.2009.10.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged, 80 and over<br/>Base Sequence<br/>Child<br/>DNA Mutational Analysis<br/>Female<br/>Fragile X Mental Retardation Protein--genetics<br/>Fragile X Syndrome--genetics<br/>Genetic Predisposition to Disease<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Molecular Sequence Data<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single Nucleotide--genetics<br/>Pregnancy<br/>Promoter Regions, Genetic--genetics