Biancalana, Valérie <br/><br/>
Five years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study reporting 95% of the activity in France.  [electronic resource] 

 -  American journal of medical genetics. Part A  Sep 2004 
 - 218-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.30237  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age Factors<br/>Blotting, Southern<br/>Child<br/>Female<br/>Fragile X Syndrome--genetics<br/>France<br/>Genetic Testing--methods<br/>Humans<br/>Male<br/>Polymerase Chain Reaction<br/>Sensitivity and Specificity<br/>Sex Factors