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B J O'Roak

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Nature Communications|November 25, 2014
Recurrent de novo mutations implicate novel genes underlying simplex autism riskB J O'Roak, H A Stessman, E A Boyle, et al.
Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.
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Showing results (1-10 of 2) with videos related to

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Pageof 1
Nature Communications|November 25, 2014
Recurrent de novo mutations implicate novel genes underlying simplex autism riskB J O'Roak, H A Stessman, E A Boyle, et al.
Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.
Pageof 1