Hereditary Spastic Paraplegia:Advances in Genetic Research
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992
Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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Retinitis Pigmentosa
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