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An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

Matthew S. Lebo, W. Chung, M. Wheeler, 2020, Human mutation.

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing

Wendy K Chung, W. Chung, S. Bale, 2015, Genetics in Medicine.

148: Increased nuchal translucency and normal karyotype: value of additional testing

V. Jobanputra, S. Bale, V. Aggarwal, 2014 .