Showing results 2 to 3 of 3
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Title | Author(s) | Issue Date | |
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Identification of TAZ mutation in a family with X-linked dilated cardiomyopathy by Next Generation Sequencing Proceeding/Conference:European Journal of Human Genetics | 2012 | ||
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics | 2014 |