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Showing articles 0 to 8 of 8 Filter Applied: molecular genetics (Click to remove) Neurofibromatosis Type 2 Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009 Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene NEJM 354:2584-2592, Case 18-2006, 2006 Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency J Pediatr 140:242-246, Wolf,B.,et al, 2002 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Showing articles 0 to 8 of 8