Showing results 1 to 9 of 9
Title | Author(s) | Issue Date | |
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2020 | |||
2022 | |||
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine | 2016 | ||
2022 | |||
Erlotinib sensitivity of MAPK1p.D321N mutation in head and neck squamous cell carcinoma Journal:npj Genomic Medicine | 2020 | ||
2018 | |||
Genetic discrimination: introducing the Asian perspective to the debate Journal:npj Genomic Medicine | 2021 | ||
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese Journal:npj Genomic Medicine | 2019 | ||
Rare versus common diseases: a false dichotomy in precision medicine Journal:npj Genomic Medicine | 2021 |