Home > Publications database > Identification and Prioritization of Causal Variants of Human Genetic Disorders from Exome or Whole Genome Sequencing Data > print

001     141835
005     20240229105132.0
024 7 _ |a 10.21926/obm.genet.1802017
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037 _ _ |a DKFZ-2018-02103
082 _ _ |a 570
100 1 _ |a Paramasivam, Nagarajan
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245 _ _ |a Identification and Prioritization of Causal Variants of Human Genetic Disorders from Exome or Whole Genome Sequencing Data
260 _ _ |a Beachwood, Ohio
|c 2018
|b Lidsen Publishing
336 7 _ |a article
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700 1 _ |a Granzow, Martin
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700 1 _ |a Evers, Christina
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700 1 _ |a Hinderhofer, Katrin
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700 1 _ |a Wiemann, Stefan
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700 1 _ |a Bartram, Claus R.
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700 1 _ |a Eils, Roland
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700 1 _ |a Schlesner, Matthias
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773 _ _ |a 10.21926/obm.genet.1802017
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910 1 _ |a Deutsches Krebsforschungszentrum
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914 1 _ |y 2018
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915 _ _ |a Creative Commons Attribution CC BY (No Version)
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