Parry, D M <br/><br/>
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.  [electronic resource] 

 -  American journal of human genetics  Sep 1996 
 - 529-39 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Cataract--genetics<br/>Genes, Neurofibromatosis 2--genetics<br/>Genotype<br/>Germ-Line Mutation--genetics<br/>Humans<br/>Male<br/>Meningioma--genetics<br/>Mutation--genetics<br/>Neurofibromatosis 2--diagnosis<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Retinal Diseases--genetics<br/>Skin Neoplasms--genetics<br/>Spinal Neoplasms--genetics