Habibi, Imen <br/><br/>
Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia.  [electronic resource] 

 -  Advances in experimental medicine and biology  2019 
 - 221-226 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0065-2598 
<br/><br/><label>Standard No.: </label>10.1007/978-3-030-27378-1_36  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anophthalmos--genetics<br/>Egypt<br/>Forkhead Transcription Factors--genetics<br/>Frameshift Mutation<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Microphthalmos--genetics<br/>Mutation<br/>Phenotype<br/>SOXB1 Transcription Factors--genetics<br/>Sequence Deletion<br/>Transcription Factors--genetics