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Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia Neerman Arbez, Marguerite; Honsberger, A.; Antonarakis, Stylianos; Morris, Michael Andréw 1999
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The essential function of Not1 lies within the Ccr4-Not complex Maillet, Laurent Jean Marie; Tu, Chi; Hong, Y K; Shuster, E O; Collart, Martine 2000
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Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5 Wider, C.; Melquist, S.; Hauf, M.; Solida, A.; ... Vingerhoets, François 2008
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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Jacquemont, Sébastien 2011
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An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium 2012