Travessa, André <br/><br/>
Prenatal diagnosis of holoprosencephaly associated with Smith-Lemli-Opitz syndrome (SLOS) in a 46,XX fetus.  [electronic resource] 

 -  Taiwanese journal of obstetrics & gynecology  Aug 2017 
 - 541-544 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1875-6263 
<br/><br/><label>Standard No.: </label>10.1016/j.tjog.2017.01.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amniotic Fluid--chemistry<br/>Cholestadienols--analysis<br/>Chorionic Villi Sampling<br/>Dehydrocholesterols--analysis<br/>Diagnosis, Differential<br/>Female<br/>Holoprosencephaly--diagnosis<br/>Homozygote<br/>Humans<br/>Karyotype<br/>Mutation<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Smith-Lemli-Opitz Syndrome--diagnosis