Waye, J S <br/><br/>
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada.  [electronic resource] 

 -  Journal of medical genetics  Jun 2002 
 - E31 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.39.6.e31  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Canada<br/>Gene Frequency<br/>Genetic Carrier Screening<br/>Humans<br/>Mutation<br/>Oxidoreductases--genetics<br/>Oxidoreductases Acting on CH-CH Group Donors<br/>Polymorphism, Single Nucleotide<br/>Smith-Lemli-Opitz Syndrome--genetics