Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine | 2016 | ||
Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay Journal:Journal of Medical Genetics | 2018 | ||
2017 |