Miguet, Marguerite <br/><br/>
Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features.  [electronic resource] 

 -  Prenatal diagnosis  Dec 2016 
 - 1276-1279 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.4965  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Craniofacial Abnormalities--genetics<br/>Female<br/>Fetal Death<br/>Gestational Age<br/>Humans<br/>Ichthyosis--embryology<br/>Male<br/>Mutation<br/>Pregnancy<br/>Trichothiodystrophy Syndromes--genetics<br/>Xeroderma Pigmentosum Group D Protein--genetics