Schaub, M <br/><br/>
[Prenatal diagnosis of Prader-Willi syndrome with CGH-Array: About a case].  [electronic resource] 

 -  Gynecologie, obstetrique, fertilite & senologie  11 2018 
 - 747-749 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>2468-7189 
<br/><br/><label>Standard No.: </label>10.1016/j.gofs.2018.09.010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosomes, Human, Pair 15<br/>Female<br/>Gene Deletion<br/>Gestational Age<br/>Humans<br/>Prader-Willi Syndrome--diagnosis<br/>Pregnancy<br/>Prenatal Diagnosis--methods