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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996
See this aricle in Pubmed

Article Abstract
These results indicate that clinical abnormalities can be present in young but absent in middle-aged presymptomatic NF2 mutation carriers.By identifying presymptomatic NF2 mutation carriers,DNA diagnosis of NF2 can improve genetic counseling and clinical management and possibly reduce psychosocial difficulties in at-risk individuals.
 
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