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Dive into the research topics of 'Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives'. Together they form a unique fingerprint.- Sort by
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Alexandre Bureau, Samuel G. Younkin, Margaret M. Parker, Joan E. Bailey-Wilson, Mary L. Marazita, Jeffrey C. Murray, Elisabeth Mangold, Hasan Albacha-Hejazi, Terri H. Beaty, Ingo Ruczinski
Research output: Contribution to journal › Article › peer-review