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Isabelle Schrauwen, Manou Sommen, Jason J. Corneveaux, Rebecca A. Reiman, Nicole J. Hackett, Charlotte Claes, Kathleen Claes, Maria Bitner‐Glindzicz, Paul Coucke, Guy Van Camp & Matthew J. Huentelman. (2012) A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR‐based approach and next generation sequencing. American Journal of Medical Genetics Part A 161:1, pages 145-152.
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Chee-Seng Ku, David N. Cooper, Constantin Polychronakos, Nasheen Naidoo, Mengchu Wu & Richie Soong. (2012) Exome sequencing: Dual role as a discovery and diagnostic tool. Annals of Neurology 71:1, pages 5-14.
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