Marcorelles, Pascale <br/><br/>
Unusual variant of holoprosencephaly in monosomy 13q.  [electronic resource] 

 -  Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society   
 - 170-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1093-5266 
<br/><br/><label>Standard No.: </label>10.1007/s10024001-0200-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Cerebral Cortex--abnormalities<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 13<br/>Female<br/>Holoprosencephaly--genetics<br/>Humans<br/>Male<br/>Nuclear Proteins<br/>Pregnancy<br/>Syndrome<br/>Transcription Factors--genetics