Showing results 1 to 5 of 5
Title | Author(s) | Issue Date | Views | |
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22q11.2 deletion syndrome in adult Chinese Patients with Conotruncal Anomalies: dysmorphisms, clinical features and underdiagnosis Proceeding/Conference:Hong Kong Journal of Paediatrics (New series) | 2013 | |||
Clinical implications of large rare copy number variations in 110 Chinese patients with conotruncal heart disease Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014 | 2014 | 48 | ||
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine | 2016 | 90 | ||
Management and outcome of antenatally diagnosed congenital cystic adenomatoid malformation of the lung Journal:Hong Kong Medical Journal | 2007 | |||
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics | 2014 | 108 |