Puissant, H <br/><br/>
Molecular analysis of 53 fragile X families with the probe StB12.3.  [electronic resource] 

 -  American journal of medical genetics  Dec 1994 
 - 370-3 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320530413  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>DNA Probes<br/>Family Health<br/>Female<br/>Fragile X Syndrome--diagnosis<br/>Genetic Linkage<br/>Genetic Markers<br/>Heterozygote<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Pregnancy<br/>Prenatal Diagnosis