Malmgren, H <br/><br/>
Methylation and mutation patterns in the fragile X syndrome.  [electronic resource] 

 -  American journal of medical genetics   
 - 268-78 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320430142  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA Mutational Analysis<br/>DNA Probes<br/>Diseases in Twins--genetics<br/>Female<br/>Fragile X Syndrome--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Methylation<br/>Pedigree<br/>Phenotype<br/>Twins, Monozygotic