Chandra, Aman <br/><br/>
Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4.  [electronic resource] 

 -  Ophthalmic genetics   
 - 78-82 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1744-5094 
<br/><br/><label>Standard No.: </label>10.3109/13816810.2012.710707  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ADAMTS Proteins<br/>Base Sequence<br/>Craniosynostoses--genetics<br/>Ectopia Lentis--genetics<br/>Exons--genetics<br/>Female<br/>Homozygote<br/>Humans<br/>Infant<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>Sequence Deletion<br/>Thrombospondins--genetics