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Evolution and functional impact of rare coding variation from deep sequencing of human exomes JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ... science 337 (6090), 64-69, 2012 | 1886 | 2012 |
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Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome J Celli, P Duijf, BCJ Hamel, M Bamshad, B Kramer, APT Smits, ... Cell 99 (2), 143-153, 1999 | 858 | 1999 |
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