Choi, Y M <br/><br/>
Carrier detection and prenatal diagnosis of hemophilia A in a Korean population by PCR-based analysis of the BclI/intron 18 and St14 VNTR polymorphisms.  [electronic resource] 

 -  Journal of human genetics  2000 
 - 218-23 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1434-5161 
<br/><br/><label>Standard No.: </label>10.1007/s100380070030  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA--analysis<br/>Factor VIII--genetics<br/>Female<br/>Genetic Carrier Screening<br/>Hemophilia A--genetics<br/>Humans<br/>Introns<br/>Korea<br/>Male<br/>Minisatellite Repeats<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Pregnancy<br/>Prenatal Diagnosis