Guaragna-Filho, Guilherme <br/><br/>
46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene.  [electronic resource] 

 -  Arquivos brasileiros de endocrinologia e metabologia  Nov 2012 
 - 578-85 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1677-9487 
<br/><br/><label>Standard No.: </label>10.1590/s0004-27302012000800020  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antley-Bixler Syndrome Phenotype--genetics<br/>Child<br/>Female<br/>Gonadal Dysgenesis, 46,XX--genetics<br/>Heterozygote<br/>Humans<br/>Mutation--genetics<br/>NADPH-Ferrihemoprotein Reductase--genetics