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000141835 245__ $$aIdentification and Prioritization of Causal Variants of Human Genetic Disorders from Exome or Whole Genome Sequencing Data
000141835 260__ $$aBeachwood, Ohio$$bLidsen Publishing$$c2018
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000141835 7001_ $$aGranzow, Martin$$b1
000141835 7001_ $$aEvers, Christina$$b2
000141835 7001_ $$aHinderhofer, Katrin$$b3
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000141835 7001_ $$aBartram, Claus R.$$b5
000141835 7001_ $$0P:(DE-He78)78b6aa82148e60b4d91e3a37a6d3d9a0$$aEils, Roland$$b6$$udkfz
000141835 7001_ $$0P:(DE-He78)f2a782242acf94a3114d75c45dc75b37$$aSchlesner, Matthias$$b7$$eLast author$$udkfz
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