Green, J S <br/><br/>
Congenital cataract with microcornea and Peters' anomaly as expressions of one autosomal dominant gene.  [electronic resource] 

 -  Ophthalmic paediatrics and genetics  Dec 1986 
 - 187-94 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0167-6784 
<br/><br/><label>Standard No.: </label>10.3109/13816818609004137  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cataract--genetics<br/>Child<br/>Chromosome Aberrations--genetics<br/>Chromosome Disorders<br/>Cornea--abnormalities<br/>Corneal Opacity--genetics<br/>Corneal Transplantation<br/>Gene Expression Regulation<br/>Genes, Dominant<br/>Humans<br/>Male<br/>Pedigree<br/>Tissue Adhesions