October 2022Our paper on an AFF3 variant in causing isolated syndactyly is out in Clinical Genetics. Congrats Glenn and Angie!
Our paper on an AFF3 variant in causing isolated syndactyly is out in Clinical Genetics. Congrats Glenn and Angie!
June 2022Our paper on maternal role of Smchd1 is out in Nature Communications!We find that maternal Smchd1 epigenetically regulates the expression of zygotic genes in the developing embryo.NUS research brings new light to unsolved genetic diseases in childrenInterview on CNA938 Health Matters with Daniel Martin
Our paper on maternal role of Smchd1 is out in Nature Communications!We find that maternal Smchd1 epigenetically regulates the expression of zygotic genes in the developing embryo.NUS research brings new light to unsolved genetic diseases in childrenInterview on CNA938 Health Matters with Daniel Martin