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Application of whole exome sequencing to identify disease-causing variants in inherited human diseases

Gerald Goh1, Murim Choi

  • 1Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA.

Genomics & Informatics
|January 25, 2013
PubMed

Keywords:
discovery of disease-causing variantsinherited human diseasenext-generation sequencingwhole exome sequencing

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