Publications

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Author Title [ Year(Desc)]
Filters: Author is Zhang, Wenjuan and Keyword is Whole Exome Sequencing  [Clear All Filters]
2017
Zieba, J. et al. A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis. Sci Rep 7, 41803 (2017).
2018
Zhang, W. et al. Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Hum Mutat 39, 152-166 (2018).