Connection
Michael Finn to Point Mutation
This is a "connection" page, showing publications Michael Finn has written about Point Mutation.
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0.014 |
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Wait SD, Vortmeyer AO, Lonser RR, Chang DT, Finn MA, Bhowmick DA, Pack SD, Oldfield EH, Zhuang Z. Somatic mutations in VHL germline deletion kindred correlate with mild phenotype. Ann Neurol. 2004 Feb; 55(2):236-40.
Score: 0.014