Kennerknecht, I <br/><br/>
How can the frequency of false-negative findings in prenatal diagnoses of fra(X) be reduced: experience with first trimester chorionic villi sampling.  [electronic resource] 

 -  American journal of medical genetics   
 - 467-75 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.1320380266  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chorionic Villi Sampling<br/>Culture Media--pharmacology<br/>False Negative Reactions<br/>Female<br/>Fibroblasts--ultrastructure<br/>Fragile X Syndrome--diagnosis<br/>Genetic Carrier Screening<br/>Genetic Markers<br/>Humans<br/>Infant, Newborn<br/>Lymphocytes--ultrastructure<br/>Male<br/>Pedigree<br/>Pregnancy<br/>Pregnancy Trimester, First<br/>Recombination, Genetic