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Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.Nature Genetics|December 11, 2012
Emergence and global spread of epidemic healthcare-associated Clostridium difficileMiao He, Fabio Miyajima, Paul Roberts, et al.Nature Genetics|May 1, 2012
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndromeDavid A Koolen, Jamie M Kramer, Kornelia Neveling, et al.Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.Nature Genetics|May 1, 2012
Meta-analysis identifies six new susceptibility loci for atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Christine M Albert, et al.Nature Genetics|May 1, 2012
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotypeMarcella Zollino, Daniela Orteschi, Marina Murdolo, et al.Nature Genetics|April 17, 2012
Common variants at 12q14 and 12q24 are associated with hippocampal volumeJoshua C Bis, Charles DeCarli, Albert Vernon Smith, et al.Nature Genetics|June 5, 2012
Maize HapMap2 identifies extant variation from a genome in fluxJer-Ming Chia, Chi Song, Peter J Bradbury, et al.Nature Genetics|May 30, 2012
The '3Is' of animal experimentationNature Genetics|May 22, 2012
Dominant missense mutations in ABCC9 cause Cantú syndromeMagdalena Harakalova, Jeske J T van Harssel, Paulien A Terhal, et al.Pageof 744