Ciara, E <br/><br/>
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome.  [electronic resource] 

 -  Clinical genetics  Dec 2004 
 - 517-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2004.00350.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Genotype<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Oxidoreductases Acting on CH-CH Group Donors--genetics<br/>Phenotype<br/>Poland<br/>Smith-Lemli-Opitz Syndrome--genetics