Publications

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Author Title [ Year(Asc)]
Filters: Author is Chong, Jessica X and Keyword is Databases, Factual  [Clear All Filters]
2017
Boycott, K. M. et al. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. Am J Hum Genet 100, 695-705 (2017).
2016
Chong, J. X. et al. Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features. Genet Med 18, 788-95 (2016).