Raymond P. Roos to Pedigree
This is a "connection" page, showing publications Raymond P. Roos has written about Pedigree.
Connection Strength
0.101
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A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep; 4(3):162-6.
Score: 0.050
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Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family. Muscle Nerve. 1993 Dec; 16(12):1416.
Score: 0.025
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Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease. Am J Med Genet. 2001 Dec 08; 105(8):737-44.
Score: 0.011
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Intrafamilial heterogeneity in hereditary motor neuron disease. Neurology. 1992 Aug; 42(8):1488-92.
Score: 0.006
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Linkage analysis in familial amyotrophic lateral sclerosis. Neurology. 1989 Jul; 39(7):919-25.
Score: 0.005
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Genetic linkage studies in Huntington disease. Cytogenet Cell Genet. 1978; 22(1-6):640-5.
Score: 0.002
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Creutzfeldt-Jakob disease: a case-control study. Am J Epidemiol. 1973 Nov; 98(5):381-94.
Score: 0.002