Alkuraya, Fowzan S <br/><br/>
Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?  [electronic resource] 

 -  Birth defects research. Part A, Clinical and molecular teratology  Aug 2005 
 - 569-71 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1542-0752 
<br/><br/><label>Standard No.: </label>10.1002/bdra.20165  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Chromosomes, Human, Pair 13<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Oxidoreductases Acting on CH-CH Group Donors--genetics<br/>Smith-Lemli-Opitz Syndrome--diagnosis<br/>Trisomy--diagnosis