Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies (Q34558011)

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Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies
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    Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies (English)
    17 January 2013
    e1003143

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