Akhtar, S <br/><br/>
Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene.  [electronic resource] 

 -  Eye (London, England)  Feb 2005 
 - 198-204 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0950-222X 
<br/><br/><label>Standard No.: </label>10.1038/sj.eye.6701453  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyloid--analysis<br/>Antigens, Neoplasm--genetics<br/>Base Sequence<br/>Cell Adhesion Molecules--genetics<br/>Cornea--chemistry<br/>Corneal Dystrophies, Hereditary--genetics<br/>Developmental Disabilities--genetics<br/>Extracellular Matrix Proteins--metabolism<br/>Female<br/>Humans<br/>Infant<br/>Lactoferrin--metabolism<br/>Male<br/>Microscopy, Immunoelectron<br/>Pedigree<br/>Polymorphism, Genetic<br/>Sequence Analysis, DNA<br/>Transforming Growth Factor beta--metabolism