Shomrat, R <br/><br/>
Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.  [electronic resource] 

 -  American journal of medical genetics  Feb 1992 
 - 281-7 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.1320420304  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Clinical Enzyme Tests<br/>Creatine Kinase--blood<br/>DNA--genetics<br/>Dystrophin--genetics<br/>Female<br/>Genetic Carrier Screening--methods<br/>Genetic Markers--genetics<br/>Humans<br/>Male<br/>Molecular Probes<br/>Muscular Dystrophies--diagnosis<br/>Pregnancy<br/>Prenatal Diagnosis--methods