Tocyap, Mary Lillian <br/><br/>
Clinical and molecular characterization of a patient with an interstitial deletion of chromosome 12q15-q23 and peripheral corneal abnormalities.  [electronic resource] 

 -  American journal of ophthalmology  Mar 2006 
 - 566-567 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>0002-9394 
<br/><br/><label>Standard No.: </label>10.1016/j.ajo.2005.09.024  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Calcineurin--genetics<br/>Carrier Proteins--genetics<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 12--genetics<br/>Cornea--abnormalities<br/>Corneal Dystrophies, Hereditary--genetics<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Microsatellite Repeats<br/>Myopia--genetics<br/>Proteoglycans--genetics