Delahaye, Andrée <br/><br/>
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.  [electronic resource] 

 -  American journal of medical genetics. Part A  Oct 2012 
 - 2430-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35548  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anterior Eye Segment--abnormalities<br/>Cerebellar Diseases--genetics<br/>Child, Preschool<br/>Chromosomes, Human, Pair 6--genetics<br/>Comparative Genomic Hybridization<br/>Dandy-Walker Syndrome--genetics<br/>Eye Abnormalities--genetics<br/>Eye Diseases, Hereditary<br/>Female<br/>Fetus--pathology<br/>Forkhead Transcription Factors--genetics<br/>Gene Deletion<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Phenotype<br/>Pregnancy