Le Brun Keris, Yann <br/><br/>
Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome.  [electronic resource] 

 -  European journal of medical genetics   
 - 472-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1769-7212 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2008.04.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Basal Cell Nevus Syndrome--diagnosis<br/>Corpus Callosum--pathology<br/>Craniofacial Abnormalities--diagnosis<br/>Exons<br/>Family Health<br/>Female<br/>Gene Deletion<br/>Humans<br/>Mutation<br/>Patched Receptors<br/>Patched-1 Receptor<br/>Pedigree<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Receptor, Melanocortin, Type 1--genetics<br/>Receptors, Cell Surface--genetics