Milà, M <br/><br/>
Rare variants in the promoter of the fragile X syndrome gene (FMR1).  [electronic resource] 

 -  Molecular and cellular probes  Apr 2000 
 - 115-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0890-8508 
<br/><br/><label>Standard No.: </label>10.1006/mcpr.2000.0293  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Case-Control Studies<br/>CpG Islands<br/>Deoxyribonucleases, Type II Site-Specific--genetics<br/>Female<br/>Fragile X Mental Retardation Protein<br/>Fragile X Syndrome--genetics<br/>Genes, Reporter<br/>Genetic Variation<br/>Humans<br/>Male<br/>Middle Aged<br/>Nerve Tissue Proteins--genetics<br/>Point Mutation<br/>Promoter Regions, Genetic<br/>RNA-Binding Proteins<br/>Recombinant Proteins--genetics<br/>Trinucleotide Repeats