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Showing articles 0 to 8 of 8 Filter Applied: genetic linkage (Click to remove) Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree JAMA 270:2316-2320, MacCollin,M.,et al, 1993 Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990 The Molecular Genetic Revolution, Its Impact on Clinical Neurology Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988 Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q Arch Neurol 56:721-726, Matsuo,H.,et al, 1999 Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992 Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis Ann Neurol 31:555-561, Gutmann,D.H.&Collins,F.S., 1992 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Showing articles 0 to 8 of 8