Al-Owain, M <br/><br/>
Smith-Lemli-Opitz syndrome among Arabs.  [electronic resource] 

 -  Clinical genetics  Aug 2012 
 - 165-72 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2011.01742.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arabs--genetics<br/>Child<br/>Child, Preschool<br/>Consanguinity<br/>Exons<br/>Facies<br/>Female<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Oxidoreductases Acting on CH-CH Group Donors--genetics<br/>Pedigree<br/>Phenotype<br/>Smith-Lemli-Opitz Syndrome--diagnosis